HU214279B - Amidvegyületeket vagy sóikat tartalmazó inszekticid készítmények és eljárás rovarkártevők ezekkel történő irtására - Google Patents
Amidvegyületeket vagy sóikat tartalmazó inszekticid készítmények és eljárás rovarkártevők ezekkel történő irtására Download PDFInfo
- Publication number
- HU214279B HU214279B HU9302144A HU9302144A HU214279B HU 214279 B HU214279 B HU 214279B HU 9302144 A HU9302144 A HU 9302144A HU 9302144 A HU9302144 A HU 9302144A HU 214279 B HU214279 B HU 214279B
- Authority
- HU
- Hungary
- Prior art keywords
- substituted
- group
- alkyl
- trifluoromethyl
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/61—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/89—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
száma | X | R1 | R2 | m | Fizikai sajátságai |
1. | 0 | -ch2cn | H | 0 | op.155-161 C° |
2. | 0 | -ch2csnh2 | H | 0 | op. 190,5-193,5 °C |
3. | 0 | -ch2oc2h5 | H | 0 | amorf szilárd anyag |
4. | 0 | -CH2NH-C3H7 (i) | H | 0 | op. 119,8C° |
5. | 0 | H | H | 0 | op. 162,7 C° |
6. | 0 | -CH2CN | 4-(trifluor-metil)-nikotinoil 0 | op.116-123C° | |
7. | 0 | -ch2cn | -coch3 | 0 | olaj |
8. | 0 | -ch2cn | -ch3 | 0 | ηθ’2 =1,4883 |
9. | 0 | -C(S)OCH3 | H | 0 | op. 138-141,5 C° |
10. | 0 | -ch3 | H | 0 | op. 83-89 C° |
11. | 0 | -CH2N(CH3)2 | H | 0 | op. 50-58 C° |
12. | 0 | 1-piperidinil-metil | H | 0 | op. 195-200 C° |
13. | 0 | -ch2cn | -CH2OC(O)C(CH3)3 | 0 | olaj |
14. | 0 | metoxi-(metil-tio)-metilén | 0 | olaj | |
15. | 0 | -CH2OH | H | 0 | op.105-113 C° |
16. | 0 | -coch3 | H | 0 | op.114-119 C° |
A vegyület | R2 | m | Fizikai sajátságai | ||
száma | X | R1 | |||
17. | 0 | -CO2CH3 | H | 0 | op. 118-128C° |
18. | 0 | 4-(trifluor-metil)-benzil | H | 0 | op.145-148 C° |
19. | 0 | 4-[4(metil-tio)-fenoxi]-benzil | H | 0 | op.103-106C° |
20. | 0 | 3-(trifluor-metil)-benzil | H | 0 | op. 76,5-78,5 C° |
21. | 0 | -CH2-C=CH | H | 0 | op. 108,5-109,5 C° |
22. | 0 | -ch2ch=ch2 | H | 0 | op. 75,5-77 C° |
23. | 0 | fenetil | H | 0 | op. 110-111 C° |
24. | 0 | -ch2ch2och3 | H | 0 | op. 56,5-59 C° |
25. | 0 | -ch2ch2ch2ch3 | H | 0 | op. 47,7 C° |
26. | 0 | ciklopropil | H | 0 | op. 105,1 C° |
27. | 0 | izobutil | H | 0 | op. 90,6 C° |
28. | 0 | -CH2-ciklopropil | H | 0 | op. 90,6 C° |
29. | 0 | -CH2CH2CN | H | 0 | op. 93,1 C° |
30. | 0 | -ch2conh2 | H | 0 | op. 155-158,5 C° |
31. | 0 | -ch2sch3 | H | 0 | op. 106,4 C° |
32. | 0 | 2-(etoxi-imino)-etil | H | 0 | op. 64,5-66 C° |
33. | 0 | -ch2oc2h5 | -CH2OC2H5 | 0 | ηθ2,4 =1,4648 |
34. | 0 | -ch2cn | -co2ch3 | 0 | olaj |
35. | 0 | -ch3 | -ch3 | 0 | ηθ’θ =1,4717 |
36. | 0 | -CH2CH(OH)CH3 | H | 0 | op. 94,9 C° |
37. | 0 | -ch2ch2oh | H | 0 | op. 101,5 C° |
38. | 0 | -ch2co2ch3 | H | 0 | op. 77,9 C° |
39. | 0 | -ch2coch3 | H | 0 | op. 112,7 C° |
40. | 0 | benzoil-metil | H | 0 | op. 144,2 C° |
41. | 0 | -CH2C=CCH2CH3 | H | 0 | op. 87,9 C° |
42. | 0 | 1 -(4-klór-fenil)-etil | H | 0 | op. 107-112 C° |
43. | 0 | -CH2CH(OC2H5)2 | H | 0 | op. 73-77 C° |
44. | 0 | -ch2cn | -CH2OCH3 | 0 | olaj |
45. | 0 | -ch2cn | -so2ch3 | 0 | olaj |
46. | 0 | -C(S)SC2H5 | H | 0 | op. 83-85 C° |
47. | 0 | (metil-tio)-(etil-tio)-metilén | 0 | op. 30-33 C° | |
48. | 0 | metoxi-(etil-tio)-metilén | 0 | op. 30-32 C° | |
49. | 0 | -CO2CH3 | -CO2CH3 | 0 | op. 67-87 C° |
50. | 0 | -ch2cho | H | 0 | amorf szilárd anyag |
51. | 0 | di(etil-tio)-metilén | 0 | op. 46,5^48,0 C° | |
52. | 0 | 2-klór-benzil | H | 0 | op. 123-124 C° |
53. | 0 | 4-klór-benzil | H | 0 | op. 161-163 C° |
54. | 0 | 3-klór-benzil | H | 0 | op. 105,5-108 C° |
55. | 0 | 2-metoxi-benzil | H | 0 | op. 119,5-123,5 C° |
56. | 0 | 4-metoxi-benzil | H | 0 | op. 140,5-143 C° |
57. | 0 | 4-nitro-benzil | H | 0 | op.165-169 C° |
58. | 0 | 4-terc-butil-benzil | H | 0 | op. 65-67 C° |
59. | 0 | 2-nitro-benzil | H | 0 | op. 127-133 C° |
60. | 0 | o-xilil | H | 0 | op. 130-132 C° |
61. | 0 | m-xilil | H | 0 | op. 92-94 C° |
62. | 0 | 2-(trifluor-metil)-benzil | H | 0 | op. 115,5-117 C° |
63. | 0 | -CH2CH2N(CH3)2 | H | 0 | op. 94,5-96,5 C° |
64. | 0 | -ch2ch3 | H | 0 | op. 85-86 C° |
65. | 0 | -piperidino-etil | H | 0 | op. 82-83 C° |
66. | 0 | 2-fenoxi-etil | H | 0 | op. 112-113,3 C° |
67. | 0 | pirid-2-il-amino | H | 0 | olaj |
68. | 0 | -CH(CH2CH3)CN | H | 0 | olaj |
69. | 0 | ciklopentil | H | 0 | op. 115C° |
70. | 0 | ciklohexil | H | 0 | op. 112,4 C° |
71. | 0 | -CH2C(CH3)3 | H | 0 | op. 87,7 C° |
72. | 0 | -CH2C(NH2)=NH | H | 0 | op.166-169 C° |
A vegyület | R2 | m | Fizikai sajátságai | ||
száma | X | R1 | |||
73. | 0 | -CH2CONHC(CH3)3 | Η | 0 | op. 158-160 C° |
74. | 0 | -ch2so2ch3 | H | 0 | op. 198-203 C° |
75. | 0 | 2-[4-(trifluor-metil)-pirid-2-il- karboxi]-etil | H | 0 | op. 121,2 C° |
76. | 0 | -CH2CH(OCH3)2 | H | 0 | op. 123,1 C° |
77. | 0 | -CH2CH2CH2C=CH | H | 0 | οπ. 73 X° |
78. | 0 | -CH2CH=C(CH3)2 | H | 0 | op. 62-66 C° |
79. | 0 | -CH2CH2-O-CH2CH2 | 0 | n·8 =1,4922 | |
80. | 0 | -CH2CH2-N(CH3)-CH2CH2- | 0 | nj,1'0 =1,4476 | |
81. | 0 | 4-metil-benzil | H | 0 | op. 143-146 C° |
82. | 0 | -ch2cf3 | H | 0 | op. 119,5-121 C° |
83. | 0 | l,2-dimetil-l-(metoxi-karbonil)-propil | H | 0 | op. 115-116 C° |
84. | 0 | -C(CH3)3 | H | 0 | op. 104,8 C° |
85. | 0 | pirrolidino-metil | H | 0 | op. 107-110 C° |
86. | 0 | morfolino-metil | H | 0 | op. 143-146 C° |
87. | 0 | 4-metil-piperazino-metil | H | 0 | op. 155-157 C° |
88. | 0 | 3,5-dimetil-morfolino-metil | H | 0 | op. 166-171 C° |
89. | s | H | H | 0 | op. 143-147 C° |
90. | s | -CH2CN | H | 0 | |
91. | 0 | 4-fenil-piperazino-metil | H | 0 | op.142-146 C° |
92. | 0 | pirrolidino-metil | -ch3 | 0 | |
93. | 0 | piperidino-metil | -c2h5 | 0 | |
94. | 0 | -CH2N(CH3)2 | -ch3 | 0 | |
95. | 0 | -CH2Si(CH3)3 | H | 0 | |
96. | 0 | 4-(piridin-2-il)-piperazino-metil | H | 0 | |
97. | 0 | 4-[5-(trifluor-metil)-piridin-2-il]- -piperazino-metil | H | 0 | |
98. | 0 | 4-metil-piperazino-metil | -ch3 | 0 | |
99. | 0 | 4-(trifluor-metil)-nikotinoil-amido-etil | H | 0 | op. 271-275 C° |
100. | 0 | N-metil-N-[4-(trifluor-metil)-niko- tinoil]-amino-etil | -ch3 | 0 | |
101. | 0 | 4-(trifluor-metil)-nikotinoil-amido- -etoxi-etil | H | 0 | |
102. | 0 | -SO2CH3 | H | 0 | op. 67-75 C° amorf |
103. | 0 | -CH2OCOC(CH3)3 | H | 0 | op. 142-145 C° |
104. | 0 | -coch3 | coch3 | 0 | op. 68-72 C° |
105. | 0 | -SO2N(CH3)2 | H | 0 | op. 172-174 C° |
106. | 0 | -conhch3 | H | 0 | op. 161-164,5 C° |
107. | 0 | -ch3 | -COCH3 | 0 | op. 49-51 C° |
108. | 0 | -ch3 | -co2ch3 | 0 | op. 44-46 C° Πβ2,4 =1,5344 |
109. | 0 | -ch2sch3 , | -ch2sch3 | 0 | |
110. | 0 | NC-N=C-N(CH)3-CH2- | ch2- | 0 | op. 160-163 C° |
111. | 0 | H | H | 1 | op. 198,8 C° |
112. | 0 | -CH3 | H | 1 | op. 119-127 C° |
113. | 0 | -ch2ch3 | H | 1 | |
114. | 0 | -ch2cn | H | 1 | op. 155-156,5 C° |
115. | 0 | piperidino-metil | H | 1 | |
116. | 0 | pirrolidino-metil | H | 1 |
Claims (6)
- SZABADALMI IGÉNYPONTOK1. Inszekticid készítmény, azzal jellemezve, hogy 0,033 - 95 tömeg% (I) általános képletű amidvegyületet - ebben a képletbenX jelentése oxigén- vagy kénatom;Y jelentése halogén- (1-
- 2 szénatomos alkil)-csoport;R1 és R2 jelentése egymástól függetlenül hidrogénatom, helyettesítetlen vagy helyettesített 1-6 szénatomos al5 kil-, 2-6 szénatomos alkenil-, 2-6 szénatomos alkinilvagy 3-8 szénatomos cikloalkilcsoport, mi mellett ezekben a csoportokban a helyettesítő halogénatom, hidroxil-, ciano-, 1-4 szénatomos alkoxi-, 1-4 szénatomos alkil-tio-, imino-, amino-, egy vagy két 1—410 szénatomos alkilcsoporttal szubsztituált amino-, 3-6 szénatomos cikloalkil vagy fenilcsoport, halogénatommal, 1-4 szénatomos alkoxi-, 1—4 szénatomos halogén-alkil- vagy nitrocsoporttal helyettesített fenilcsoport, fenoxicsoport, továbbá olyan fenoxi-fenil15 csoport, amelyben a fenoxicsoport szubsztituensként1—4 szénatomos alkil-tio-csoportot hordozhat, piperidinil-, pirrolidinil-, adott esetben 1—4 szénatomos alkilcsoporttal szubsztituált morfolino-, 1-4 szénatomos alkilcsoporttal vagy fenilcsoporttal szubsztituált20 piperazinilcsoport lehet, továbbá R1 és/vagy R2 szubsztituense lehet még -C(W*)R8 képletű csoport, amelyben W1 jelentése oxigén-vagy kénatom és R8 jelentése hidrogénatom, aminocsoport, egy25 vagy két 1—4 szénatomos alkilcsoporttal helyettesített aminocsoport, 1-4 szénatomos alkil-, 1-4 szénatomos alkoxi-, 1-4 szénatomos alkiltio- vagy fenilcsoport;-OC(W')R9 képletű csoport, amelyben30 W1 jelentése egyezik a fent megadott,R9 jelentése 1-4 szénatomos alkilcsoport, 1-4 szénatomos halogén-alkil-csoporttal helyettesített piridilcsoport, vagy lehet R1 és R2 szubsztituense 1-4 szénatomos alkil35 szulfonil-csoport;R1 és R2 jelentése lehet még-C(W’)R3 képletű csoport, amelyben W1 jelentése oxigén- vagy kénatom;R3 jelentése helyettesítetlen 1—4 szénatomos al40 kil, 1-4 szénatomos alkoxi-, 1-4 szénatomos alkil-tio vagy 1—4 szénatamos alkil-aminocsoport, vagy halogén-) 1—4 szénatomos alkil)csoporttal helyettesített piridilcsoport; vagy-S(O)2 R4 képletű csoport és ebben45 R4 jelentése 1-4 szénatomos alkil-amino- vagy di( 1 —4 szénatomos alkilj-amino-csoport; vagyR1 és R2 együtt egy =C(R6)R7 képletű csoportot képez, amelyben R6 és R7 j elentése egymástól függetlenül 1—4 szénatomos alkoxi- vagy 1—4 szénatomos50 alkil-tio-csoport, vagyR1 és R2 a szomszédos nitrogénatommal együtt egy morfolino-, 4-metil-piperazinil- vagy 2-(ciano-imino)3-metil- 1-imidazolinil-csoport;m értéke 0 vagy 1 55 vagy ennek sóját tartalmazza hatóanyagként, mezőgazdasági célra alkalmas segédanyag, előnyösen vivőanyag, emulgeátor, diszpergálószer, nedvesítőszerek kíséretében.(Elsőbbsége: 1993. 07.23.)60 2. Az 1. igénypont szerinti inszekticid készítmény,HU 214 279 Β azzal jellemezve, hogy 1-95 tömeg% mennyiségben tartalmazza az (I) általános képletű amid vegyületet vagy ennek sóját - ahol R1, R2, Y és m jelentése egyezik az 1. igénypontban megadottal - segédanyag mellett.(Elsőbbsége: 1993. 07. 23.)
- 3. Az 1. igénypont szerinti inszekticid készítmény, azzal jellemezve, hogy 2,5 - 20 tömeg% mennyiségben tartalmazza az (I) általános képletű amid vegyületet vagy ennek sóját - ahol R1, R2 Y és m jelentése egyezik az 1. igénypontban megadottal segédanyag mellett.(Elsőbbsége: 1993. 07. 23.)
- 4. Eljárás rovarkártevők irtására, azzal jellemezve, hogy az 1. igénypontban meghatározott inszekticid készítményt 0,1 - 500 000 ppm hatóanyag-koncentráció5 bán alkalmazzuk a rovarkártevők ellen. (Elsőbbsége: 1993. 07. 23.)
- 5. A 4. igénypont szerinti eljárás, azzaljellemezve, hogy hatóanyagként 4-(trifluor-metil)-3-piridin-karboxamidot tartalmazó 1. igénypont szerinti inszekticid készítményt
- 10 alkalmazunk. (Elsőbbsége: 1993. 07. 23.)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP23880492 | 1992-07-23 | ||
JP5766893 | 1993-02-05 | ||
JP9642893 | 1993-03-17 |
Publications (3)
Publication Number | Publication Date |
---|---|
HU9302144D0 HU9302144D0 (en) | 1993-11-29 |
HUT68334A HUT68334A (en) | 1995-06-28 |
HU214279B true HU214279B (hu) | 1998-03-02 |
Family
ID=27296335
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU9302144A HU214279B (hu) | 1992-07-23 | 1993-07-23 | Amidvegyületeket vagy sóikat tartalmazó inszekticid készítmények és eljárás rovarkártevők ezekkel történő irtására |
Country Status (24)
Country | Link |
---|---|
US (1) | US5360806A (hu) |
EP (1) | EP0580374B1 (hu) |
JP (1) | JP2994182B2 (hu) |
KR (1) | KR100282243B1 (hu) |
CN (1) | CN1044233C (hu) |
AT (1) | ATE132489T1 (hu) |
AU (1) | AU657056B2 (hu) |
BR (1) | BR9302960A (hu) |
CA (1) | CA2100011C (hu) |
CO (1) | CO4750587A1 (hu) |
CZ (1) | CZ286147B6 (hu) |
DE (1) | DE69301205T2 (hu) |
DK (1) | DK0580374T3 (hu) |
EG (1) | EG20154A (hu) |
ES (1) | ES2085118T3 (hu) |
GR (1) | GR3018953T3 (hu) |
HK (1) | HK1001896A1 (hu) |
HU (1) | HU214279B (hu) |
IL (1) | IL106340A (hu) |
MX (1) | MX9304425A (hu) |
NL (1) | NL350027I2 (hu) |
PL (1) | PL173611B1 (hu) |
SK (1) | SK281481B6 (hu) |
TW (1) | TW242554B (hu) |
Families Citing this family (100)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL116148A (en) * | 1994-11-30 | 2001-03-19 | Rhone Poulenc Agrochimie | Complexible composition for insect control |
EP0744400B1 (en) * | 1995-05-26 | 2002-09-11 | Ishihara Sangyo Kaisha, Ltd. | Process for producing 4-trifluoromethylnicotinic acid |
US6114357A (en) * | 1995-11-13 | 2000-09-05 | Smithkline Beecham Corporation | Hemoregulatory compounds |
US6107309A (en) * | 1995-11-13 | 2000-08-22 | Smithkline Beecham Corporation | Hemoregulatory compounds |
US6030989A (en) * | 1995-11-13 | 2000-02-29 | Smithkline Beecham Corporation | Hemoregulatory compounds |
US6077856A (en) * | 1995-11-13 | 2000-06-20 | Smithkline Beecham Corporation | Hemoregulatory compounds |
NZ323207A (en) * | 1995-11-13 | 1999-11-29 | Smithkline Beecham Corp | Hemoregulatory compounds |
DE19858193A1 (de) * | 1998-12-17 | 2000-06-21 | Aventis Cropscience Gmbh | 4-Trifluormethyl-3-oxadiazolylpyridine, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel |
US6367193B1 (en) | 2000-03-17 | 2002-04-09 | North Carolina State University | Method of protecting plants from cold injury |
WO2001070692A2 (de) * | 2000-03-22 | 2001-09-27 | Bayer Cropscience Gmbh | Heterocyclische acylsulfimide,verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als schädlingsbekämpfungsmittel |
DE10017881A1 (de) * | 2000-04-11 | 2001-10-25 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
JP2002201133A (ja) * | 2000-05-25 | 2002-07-16 | Ishihara Sangyo Kaisha Ltd | 動物の外部寄生虫防除用組成物 |
AU5882201A (en) * | 2000-05-25 | 2001-12-03 | Ishihara Sangyo Kaisha Ltd. | Compositions for controlling animal ectoparasites |
TWI242006B (en) * | 2000-10-23 | 2005-10-21 | Ishihara Sangyo Kaisha | Pesticidal composition |
AU2002214045A1 (en) * | 2000-11-10 | 2002-05-21 | Syngenta Participations Ag | Synergistic pesticidal compositions comprising n-cyanomethyl-4-(trifluoromethyl)nicotinamide |
AR031658A1 (es) | 2000-12-13 | 2003-09-24 | Aventis Cropscience Gmbh | Procedimiento para la preparacion de 4-haloalquilnicotinonitrilos |
JP4554064B2 (ja) * | 2000-12-19 | 2010-09-29 | 優一郎 新崎 | 線状のブラシ用素材 |
KR100850252B1 (ko) * | 2000-12-20 | 2008-08-04 | 노파르티스 아게 | 유기 화합물 |
DE10144410A1 (de) * | 2001-09-11 | 2003-03-27 | Bayer Cropscience Gmbh | Verfahren zur Herstellung von 4-Haloalkylnicotinsäureestern |
DE10146873A1 (de) * | 2001-09-24 | 2003-04-17 | Bayer Cropscience Gmbh | Heterocyclische Amide und -Iminderivate, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel |
DE10148290A1 (de) * | 2001-09-29 | 2003-04-17 | Bayer Cropscience Gmbh | Heterocyclische Amide, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung |
TWI301400B (en) * | 2002-02-22 | 2008-10-01 | Ishihara Sangyo Kaisha | Composition for controlling house insect pest and method for controlling house insect pest |
US7476685B2 (en) * | 2002-05-16 | 2009-01-13 | Merial Limited | Pyridine carboxamide derivatives and their use as pesticides |
WO2003097605A1 (en) * | 2002-05-16 | 2003-11-27 | Bayer Cropscience Gmbh | Pesticidal pyridinecarboxamide derivatives |
DE10223274A1 (de) | 2002-05-24 | 2003-12-04 | Bayer Cropscience Gmbh | Verfahren zur Herstellung von 4-Haloalkylnicotinsäureamiden |
US7387804B2 (en) * | 2002-06-03 | 2008-06-17 | Mishima Foods Co., Ltd. | Dark opal basil leaves or extract thereof having improved storability |
US20040067985A1 (en) * | 2002-10-04 | 2004-04-08 | Fortuna Haviv | Method of inhibiting angiogenesis |
JP4792199B2 (ja) * | 2002-10-07 | 2011-10-12 | 石原産業株式会社 | 家屋害虫防除用組成物及び防除方法 |
DE10307845A1 (de) * | 2003-02-25 | 2004-09-02 | Bayer Cropscience Gmbh | Heterocyclische Amide, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel |
DE10313683A1 (de) * | 2003-03-26 | 2004-10-07 | Bayer Cropscience Ag | Substituierte Pyri(mi)din(thio)carboxamide |
DE10318690B3 (de) * | 2003-04-24 | 2004-11-11 | Merck Patent Gmbh | Verfahren zur Herstellung von Nicotinaldehyden |
US20070010532A1 (en) * | 2003-07-01 | 2007-01-11 | Bayer Cropscience Gmbh | 3-Pyridylcarboxamide derivatives as pesticidal agents |
DE10346245A1 (de) * | 2003-10-06 | 2005-04-28 | Bayer Cropscience Gmbh | Verfahren zur Herstellung von Acylharnstoffderivaten, Salze dieser Acylharnstoffderivate und deren Verwendung als Schädlingsbekämpfungsmittel |
JP2005162732A (ja) * | 2003-11-13 | 2005-06-23 | Bayer Cropscience Ag | 殺虫性ニコチノイルカーバメート類 |
JP4927553B2 (ja) * | 2003-11-13 | 2012-05-09 | ザ ニュージーランド インスティテュート フォー プラント アンド フード リサーチ リミティド | 昆虫行動修正化合物 |
MXPA06011760A (es) * | 2004-04-14 | 2006-12-15 | Fmc Corp | Composiciones pesticidas dispersables. |
DE102004022897A1 (de) * | 2004-05-10 | 2005-12-08 | Bayer Cropscience Ag | Azinyl-imidazoazine |
DE102004031323A1 (de) * | 2004-06-29 | 2006-01-19 | Bayer Cropscience Ag | Substituierte Pyridazincarboxamide und Derivate hiervon |
DE102004035134A1 (de) * | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von Halogenalkylnicotinsäurederivaten, Anthranilsäureamiden oder Phthalsäurediamiden und Safenern |
JP2008517025A (ja) * | 2004-10-22 | 2008-05-22 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺虫剤混合物 |
AU2006268785B2 (en) | 2005-07-07 | 2012-03-22 | Basf Se | N-Thio-anthranilamid compounds and their use as pesticides |
PE20071233A1 (es) * | 2006-02-16 | 2008-01-10 | Basf Ag | Compuestos de tioamida para combatir pestes animales |
JP5571387B2 (ja) | 2007-01-11 | 2014-08-13 | クリティカル・アウトカム・テクノロジーズ・インコーポレイテッド | 癌の治療のための化合物および方法 |
US8138191B2 (en) | 2007-01-11 | 2012-03-20 | Critical Outcome Technologies Inc. | Inhibitor compounds and cancer treatment methods |
JP2010523476A (ja) | 2007-03-08 | 2010-07-15 | ザ ボード オブ トラスティーズ オブ ザ リーランド スタンフォード ジュニア ユニバーシティ | ミトコンドリアアルデヒドデヒドロゲナーゼ−2モジュレーター及びその使用方法 |
JP5436211B2 (ja) * | 2007-08-10 | 2014-03-05 | クミアイ化学工業株式会社 | 有害生物防除剤組成物及び有害生物防除方法 |
DE102007045922A1 (de) | 2007-09-26 | 2009-04-02 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
WO2009079797A1 (en) | 2007-12-26 | 2009-07-02 | Critical Outcome Technologies, Inc. | Compounds and method for treatment of cancer |
JP5611535B2 (ja) * | 2008-04-17 | 2014-10-22 | 石原産業株式会社 | 有害生物防除剤組成物及び有害生物の防除方法 |
EP2127522A1 (de) | 2008-05-29 | 2009-12-02 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
JP2012502048A (ja) | 2008-09-08 | 2012-01-26 | ボード オブ トラスティーズ オブ ザ レランド スタンフォード ジュニア ユニバーシティ | アルデヒドデヒドロゲナーゼ活性のモジュレーターおよびその使用方法 |
JP2012506856A (ja) | 2008-10-28 | 2012-03-22 | ボード オブ トラスティーズ オブ ザ レランド スタンフォード ジュニア ユニバーシティ | アルデヒドデヒドロゲナーゼのモジュレーターおよびその使用方法 |
EP2227951A1 (de) | 2009-01-23 | 2010-09-15 | Bayer CropScience AG | Verwendung von Enaminocarbonylverbindungen zur Bekämpfung von durch Insekten übertragenen Viren |
PT2564698T (pt) | 2009-03-25 | 2016-08-12 | Bayer Cropscience Ag | Combinações de substâncias ativas nematicidas, compreendendo fluopiram e bacillus firmus |
WO2011120153A1 (en) | 2010-04-01 | 2011-10-06 | Critical Outcome Technologies Inc. | Compounds and method for treatment of hiv |
CN102905525A (zh) | 2010-04-27 | 2013-01-30 | 先正达参股股份有限公司 | 控制耐新烟碱的蚜虫的方法 |
EP2382865A1 (de) | 2010-04-28 | 2011-11-02 | Bayer CropScience AG | Synergistische Wirkstoffkombinationen |
UA109282C2 (xx) | 2010-07-09 | 2015-08-10 | Пестицидна суспензія на водній основі | |
JP5629881B2 (ja) | 2010-08-11 | 2014-11-26 | 住友化学株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
JP5706179B2 (ja) * | 2010-08-20 | 2015-04-22 | 住友化学株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
JP5681860B2 (ja) | 2010-08-20 | 2015-03-11 | 住友化学株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
JP5659364B2 (ja) | 2010-08-20 | 2015-01-28 | 石原産業株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
US10457659B2 (en) | 2011-04-29 | 2019-10-29 | The Board Of Trustees Of The Leland Stanford Junior University | Compositions and methods for increasing proliferation of adult salivary stem cells |
EP2564697A1 (en) * | 2011-08-29 | 2013-03-06 | Syngenta Participations AG. | Methods of controlling insects |
CN103053566A (zh) * | 2011-10-20 | 2013-04-24 | 南京华洲药业有限公司 | 一种含氟啶虫酰胺和速灭威的复合杀虫组合物及其用途 |
CN103053604A (zh) * | 2011-10-20 | 2013-04-24 | 南京华洲药业有限公司 | 一种含氟啶虫酰胺和氟硅菊酯的增效杀虫组合物及其用途 |
CN104487439B (zh) | 2012-05-24 | 2017-06-09 | 巴斯夫欧洲公司 | N‑硫代邻氨基苯甲酰胺化合物及其作为杀害虫剂的用途 |
CN102696655B (zh) * | 2012-05-24 | 2013-11-27 | 永农生物科学有限公司 | 含有螺螨酯的复配农药组合物及其制剂 |
NZ702435A (en) * | 2012-06-30 | 2016-07-29 | Dow Agrosciences Llc | Insecticidal n-substituted sulfilimine and sulfoximine pyridine n-oxides |
CN104602527B (zh) * | 2012-06-30 | 2018-09-25 | 美国陶氏益农公司 | 吡啶n-氧化物及其制备方法 |
WO2014004094A1 (en) * | 2012-06-30 | 2014-01-03 | Dow Agrosciences Llc | Production of n-substituted sulfoximine pyridine n-oxides |
WO2014054425A1 (ja) * | 2012-10-01 | 2014-04-10 | 住友化学株式会社 | アミド化合物 |
CN105358531B (zh) * | 2013-03-14 | 2017-11-14 | 利兰-斯坦福大学初级学院的董事会 | 线粒体醛脱氢酶‑2调节剂和其使用方法 |
CN103524407B (zh) * | 2013-11-01 | 2015-12-02 | 青岛农业大学 | 一组2-氟-3-吡啶甲酰化合物 |
RU2664574C1 (ru) | 2013-11-12 | 2018-08-21 | Нихон Нохияку Ко., Лтд. | Амидное соединение или его соль, сельскохозяйственный и садовый инсектицид и бактерицид, содержащие данное соединение, и способ применения данного инсектицида и бактерицида |
CN103951616B (zh) * | 2014-04-15 | 2016-03-16 | 湖南化工研究院 | N-氰甲基-4-(三氟甲基)烟酰胺的制备方法 |
CN104488925A (zh) * | 2014-12-03 | 2015-04-08 | 广东中迅农科股份有限公司 | 一种含有甾烯醇和氟啶虫酰胺的农药组合物 |
CN104824004A (zh) * | 2015-04-16 | 2015-08-12 | 广东中迅农科股份有限公司 | 一种含有异菌脲和氟啶虫酰胺的农药组合物 |
US20170094972A1 (en) | 2015-10-06 | 2017-04-06 | Syngenta Participations Ag | Compounds and Compositions Having Knock-Down Activity Against Insect Pests |
EP3183968A1 (en) | 2015-12-21 | 2017-06-28 | Ceva Sante Animale | Methods and means for the eradication of fleas |
RS65077B1 (sr) | 2017-04-05 | 2024-02-29 | Syngenta Participations Ag | Postupak i polimerna supstanca koja ima aktivnost nokdauna ili inhibicije hranjenja krvlju kod komaraca |
CN107286086B (zh) * | 2017-05-23 | 2021-04-20 | 河北科技大学 | N-氰甲基双(三氟甲基)烟酰胺的制备方法及n-氰甲基双(三氟甲基)烟酰胺的应用 |
CN107417606B (zh) * | 2017-06-12 | 2020-07-10 | 河北科技大学 | N-氰甲基双(三氟甲基)烟酰胺转化为氟啶虫酰胺的方法及应用 |
CN107382848A (zh) * | 2017-07-15 | 2017-11-24 | 河北蓝泰化工科技有限公司 | 一种烟酰胺化合物及其制备方法和应用 |
US11401271B2 (en) | 2017-11-03 | 2022-08-02 | South China Agricultural University | Fused heterocyclic compound, pyrazole-ring-containing fused heterocyclic compound, agricultural composition containing thereof, and method of using the composition |
JP2021035912A (ja) | 2017-12-20 | 2021-03-04 | 石原産業株式会社 | 有害生物防除用組成物及び有害生物の防除方法 |
JP7063231B2 (ja) * | 2018-10-26 | 2022-05-09 | 住友化学株式会社 | ジピリダジニルエーテル化合物及びその用途 |
CN110495459A (zh) * | 2019-08-06 | 2019-11-26 | 京博农化科技有限公司 | 一种氟啶虫酰胺与三十烷醇的杀虫组合物 |
CA3204864A1 (en) * | 2020-02-12 | 2021-08-19 | Upl Limited | Method of improving plant growth |
CN113826640B (zh) * | 2020-06-23 | 2024-05-03 | 江苏功成生物科技有限公司 | 一种含有氟啶虫酰胺的卫生杀虫组合物及其应用 |
CN111820220A (zh) * | 2020-08-04 | 2020-10-27 | 京博农化科技有限公司 | 一种含有氟啶虫酰胺的农药组合物及其应用 |
EP4337015A1 (en) | 2021-05-14 | 2024-03-20 | Syngenta Crop Protection AG | Insect, acarina and nematode pest control |
BR112023023835A2 (pt) | 2021-05-14 | 2024-01-30 | Syngenta Crop Protection Ag | Composições para tratamento de sementes |
WO2022268813A1 (en) | 2021-06-24 | 2022-12-29 | Syngenta Crop Protection Ag | Insect, acarina and nematode pest control |
WO2022268815A1 (en) | 2021-06-24 | 2022-12-29 | Syngenta Crop Protection Ag | Insect, acarina and nematode pest control |
CN113943249B (zh) * | 2021-11-18 | 2023-08-29 | 江苏中旗科技股份有限公司 | 一种n-氰甲基-4-(三氟甲基)烟酰胺的制备方法 |
WO2023105064A1 (en) | 2021-12-10 | 2023-06-15 | Syngenta Crop Protection Ag | Insect, acarina and nematode pest control |
CN114532355A (zh) * | 2022-03-09 | 2022-05-27 | 合肥巨卓农业科技合伙企业(有限合伙) | 一种含有二嗪磷和氟啶虫酰胺的杀虫组合物及其制备方法 |
CN114656402B (zh) * | 2022-04-11 | 2024-01-30 | 青岛科技大学 | 一种含氟烟酰脲类化合物及其用途 |
CN115925621A (zh) * | 2022-12-22 | 2023-04-07 | 山东京博农化科技股份有限公司 | 一种甘氨酸双酰胺衍生物、其制备方法及其用途 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3469520D1 (en) * | 1984-01-19 | 1988-04-07 | Ici Plc | Biologically active amide derivatives |
AR241530A1 (es) * | 1984-12-21 | 1992-08-31 | Ciba Geigy A G Cesionaria De F | 1,2,4-triazoles, composicion para el control de pestes y procedimiento para la preparacion de 1,2,4-triazoles. |
JPS63130583A (ja) * | 1986-11-18 | 1988-06-02 | Nippon Kayaku Co Ltd | イソニコチン酸アミド誘導体およびそれを有効成分とする農園芸用殺菌剤組成物 |
WO1992012133A2 (en) * | 1991-01-08 | 1992-07-23 | E.I. Du Pont De Nemours And Company | Arthropodicidal carboxanilides |
-
1993
- 1993-06-30 JP JP5214766A patent/JP2994182B2/ja not_active Expired - Lifetime
- 1993-07-06 TW TW082105377A patent/TW242554B/zh active
- 1993-07-07 CA CA002100011A patent/CA2100011C/en not_active Expired - Lifetime
- 1993-07-14 IL IL10634093A patent/IL106340A/en not_active IP Right Cessation
- 1993-07-15 SK SK750-93A patent/SK281481B6/sk active Protection Beyond IP Right Term
- 1993-07-16 ES ES93305622T patent/ES2085118T3/es not_active Expired - Lifetime
- 1993-07-16 DK DK93305622.8T patent/DK0580374T3/da active
- 1993-07-16 EP EP93305622A patent/EP0580374B1/en not_active Expired - Lifetime
- 1993-07-16 AT AT93305622T patent/ATE132489T1/de active
- 1993-07-16 DE DE69301205T patent/DE69301205T2/de not_active Expired - Lifetime
- 1993-07-21 EG EG45993A patent/EG20154A/xx active
- 1993-07-21 AU AU42106/93A patent/AU657056B2/en not_active Expired
- 1993-07-22 CO CO93397781A patent/CO4750587A1/es unknown
- 1993-07-22 BR BR9302960A patent/BR9302960A/pt not_active IP Right Cessation
- 1993-07-22 MX MX9304425A patent/MX9304425A/es unknown
- 1993-07-22 PL PL93299769A patent/PL173611B1/pl unknown
- 1993-07-22 KR KR1019930013885A patent/KR100282243B1/ko active IP Right Grant
- 1993-07-23 HU HU9302144A patent/HU214279B/hu active Protection Beyond IP Right Term
- 1993-07-23 US US08/095,192 patent/US5360806A/en not_active Expired - Lifetime
- 1993-07-23 CZ CZ19931502A patent/CZ286147B6/cs not_active IP Right Cessation
- 1993-07-23 CN CN93109092A patent/CN1044233C/zh not_active Expired - Lifetime
-
1996
- 1996-02-14 GR GR960400353T patent/GR3018953T3/el unknown
-
1998
- 1998-02-07 HK HK98100953A patent/HK1001896A1/xx not_active IP Right Cessation
-
2006
- 2006-03-21 NL NL350027C patent/NL350027I2/nl unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HU214279B (hu) | Amidvegyületeket vagy sóikat tartalmazó inszekticid készítmények és eljárás rovarkártevők ezekkel történő irtására | |
DK2256112T3 (en) | Anthranilamides, process for their production and insecticides containing the same | |
US9867372B2 (en) | Tetrazolinone compound and use of same | |
PT2030971E (pt) | Agente de controlo de pragas contendo um novo derivado de piridil-metamina ou seu sal | |
FR2928070A1 (fr) | Composition agricole, utilisation d'un compose pour sa production et procede pour matriser ou prevenir les maladies des plantes. | |
RU2049775C1 (ru) | N-фенилкарбаматное соединение и фунгицидная композиция | |
WO2021085370A1 (ja) | アゾール誘導体及びその用途 | |
JPH10324687A (ja) | ピロール化合物、製法および農園芸用殺菌剤 | |
JP2606720B2 (ja) | イミダゾール系化合物及びそれらを含有する有害生物防除剤 | |
JPH0725853A (ja) | アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 | |
JP2010513343A (ja) | 殺真菌剤としてのビスオキシム | |
JPH0710841A (ja) | 4−トリフルオロメチルピリジン−3−カルボキサミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 | |
JP2006089469A (ja) | 光学活性フタルアミド誘導体及び農園芸用殺虫剤並びにその使用方法 | |
MX2011005158A (es) | Derivado de piridina o su sal, pesticida que lo contiene y procedimiento para su produccion. | |
CN110573496A (zh) | N-(4-吡啶基)烟酰胺化合物或其盐 | |
WO1995027700A1 (fr) | Compose d'ether, son utilisation et intermediaire pour l'obtention de ce compose | |
JPWO2019168112A1 (ja) | イミド誘導体およびそれらを有効成分として含有する殺菌剤 | |
JP4121158B2 (ja) | アルコキシイミノ置換二環式誘導体を有効成分とする病害又は害虫防除剤 | |
WO1996001257A1 (fr) | Nouveau compose du type triazol, son procede de production, et agent pesticide | |
JPH10101648A (ja) | アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤 | |
JP2007070346A (ja) | アントラニルアミド系化合物、それらの製造方法及びそれらを含有する有害生物防除剤 | |
JP4799744B2 (ja) | フェナシルアミン誘導体、それらの製造方法及びそれらを含有する有害生物防除剤 | |
RU2083562C1 (ru) | Производные пиридина, способ их получения, инсектицидная композиция | |
RU2140908C1 (ru) | Производные бензамидоксима, способ их получения и фунгицидное средство для защиты сельскохозяйственных растений | |
TW202000657A (zh) | 取代吡啶化合物或其鹽 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AA1S | Information on application for a supplementary protection certificate |
Free format text: PRODUCT NAME: FLONIKAMID/FLONICAMID; NATIONAL REGISTER NO/DATE: 025/1174/4/2007*2007.11.26; FIRST REGISTRATION NO/DATE: FR*2050046*2005.04.21 Spc suppl protection certif: S0800001 Filing date: 20080107 Expiry date: 20130723 Effective date: 20080122 Free format text: PRODUCT NAME: FLONICAMID; REG. NO/DATE: 025/1174/4/2007 20071126; FIRST REG.: FR 2050046 20050421 Spc suppl protection certif: S0800001 Filing date: 20080107 Expiry date: 20130723 |
|
FG4S | Grant of supplementary protection certificate |
Free format text: PRODUCT NAME: FLONICAMID; REG. NO/DATE: 025/1174/4/2007 20071126; FIRST REG. NO: 2050046 20050421 Spc suppl protection certif: S0800001 Filing date: 20080107 Expiry date: 20130723 Extension date: 20180723 |