CS902882A2 - Insekticidni a nematocidni prostredek - Google Patents

Insekticidni a nematocidni prostredek Download PDF

Info

Publication number: CS902882A2
Authority: CS; Czechoslovakia
Prior art keywords: sup; závislosti; group; sub; methyl
Prior art date: 1981-12-10

Application number

CS829028A

Other languages

Czech (cs)

English (en)

Inventor

Mark A Dekeyser

Benjamin J Pierce

Charles R Moore

Winchester L Hubbard

Original Assignee

Uniroyal

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1981-12-10

Filing date

1982-12-10

Publication date

1985-07-16

1982-12-10 Application filed by Uniroyal filed Critical Uniroyal

1985-07-16 Publication of CS902882A2 publication Critical patent/CS902882A2/cs

Links

239000000203 mixture Substances 0.000 claims abstract description 61
150000001875 compounds Chemical class 0.000 claims abstract description 16
-1 1,3-butadien-1,4-diyl group Chemical group 0.000 claims abstract description 14
150000002903 organophosphorus compounds Chemical class 0.000 claims abstract description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 9
229910052717 sulfur Inorganic materials 0.000 claims abstract description 7
125000000217 alkyl group Chemical group 0.000 claims abstract description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 6
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 5
229910052760 oxygen Inorganic materials 0.000 claims abstract description 5
229910052799 carbon Inorganic materials 0.000 claims abstract description 4
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
239000001257 hydrogen Substances 0.000 claims abstract description 4
125000003545 alkoxy group Chemical group 0.000 claims abstract description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 3
239000001301 oxygen Substances 0.000 claims abstract description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 3
239000000460 chlorine Substances 0.000 claims description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
239000004480 active ingredient Substances 0.000 claims description 10
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
230000000749 insecticidal effect Effects 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 6
230000001069 nematicidal effect Effects 0.000 claims description 5
125000004434 sulfur atom Chemical group 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
238000000034 method Methods 0.000 abstract description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 3
241000607479 Yersinia pestis Species 0.000 abstract description 3
230000015572 biosynthetic process Effects 0.000 abstract description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
239000011593 sulfur Substances 0.000 abstract 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
150000003840 hydrochlorides Chemical class 0.000 abstract 1
239000000376 reactant Substances 0.000 abstract 1
238000003786 synthesis reaction Methods 0.000 abstract 1
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
241000196324 Embryophyta Species 0.000 description 17
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
239000002689 soil Substances 0.000 description 11
239000000126 substance Substances 0.000 description 11
239000007787 solid Substances 0.000 description 9
241000238631 Hexapoda Species 0.000 description 8
239000000543 intermediate Substances 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
239000002904 solvent Substances 0.000 description 6
239000000047 product Substances 0.000 description 5
239000004094 surface-active agent Substances 0.000 description 5
239000000725 suspension Substances 0.000 description 5
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
239000000443 aerosol Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
239000007921 spray Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
241000244206 Nematoda Species 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
238000003556 assay Methods 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000002917 insecticide Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 2
241000167882 Rhopalosiphum maidis Species 0.000 description 2
240000003768 Solanum lycopersicum Species 0.000 description 2
240000008042 Zea mays Species 0.000 description 2
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
235000002017 Zea mays subsp mays Nutrition 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
239000000969 carrier Substances 0.000 description 2
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 2
239000004927 clay Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
235000005822 corn Nutrition 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000009472 formulation Methods 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920000137 polyphosphoric acid Polymers 0.000 description 2
150000004760 silicates Chemical class 0.000 description 2
239000012265 solid product Substances 0.000 description 2
239000000758 substrate Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
PMCOWOCKUQWYRL-UHFFFAOYSA-N 2,4-dimethylpyrimidine Chemical class CC1=CC=NC(C)=N1 PMCOWOCKUQWYRL-UHFFFAOYSA-N 0.000 description 1
ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 1
NDAJNMAAXXIADY-UHFFFAOYSA-N 2-methylpropanimidamide Chemical compound CC(C)C(N)=N NDAJNMAAXXIADY-UHFFFAOYSA-N 0.000 description 1
LNJMHEJAYSYZKK-UHFFFAOYSA-N 2-methylpyrimidine Chemical class CC1=NC=CC=N1 LNJMHEJAYSYZKK-UHFFFAOYSA-N 0.000 description 1
WTAZAHLROWIQRC-UHFFFAOYSA-N 3-ethylpyridin-2-amine Chemical compound CCC1=CC=CN=C1N WTAZAHLROWIQRC-UHFFFAOYSA-N 0.000 description 1
UCTNTYHJFWMUBD-UHFFFAOYSA-N 4-chloro-3-oxobutanoic acid Chemical compound OC(=O)CC(=O)CCl UCTNTYHJFWMUBD-UHFFFAOYSA-N 0.000 description 1
WANAHALOOUKFKI-UHFFFAOYSA-N 7-(chloromethyl)-[1,3]thiazolo[3,2-a]pyrimidin-5-one Chemical compound ClCC1=CC(=O)N2C=CSC2=N1 WANAHALOOUKFKI-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
244000204909 Anoda cristata Species 0.000 description 1
241001124076 Aphididae Species 0.000 description 1
241000239290 Araneae Species 0.000 description 1
101100456566 Caenorhabditis elegans dpy-22 gene Proteins 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000489975 Diabrotica Species 0.000 description 1
241000489973 Diabrotica undecimpunctata Species 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
241000256257 Heliothis Species 0.000 description 1
241000256244 Heliothis virescens Species 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 1
NSTIECCOJUDAHW-UHFFFAOYSA-N P(=S)([S-])([O-])[O-].C[NH2+]C.C[NH2+]C.C[NH2+]C Chemical compound P(=S)([S-])([O-])[O-].C[NH2+]C.C[NH2+]C.C[NH2+]C NSTIECCOJUDAHW-UHFFFAOYSA-N 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
241000159959 Takecallis sasae Species 0.000 description 1
244000204900 Talipariti tiliaceum Species 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
PPGORMGERPBFTJ-UHFFFAOYSA-N azane;dimethoxy-sulfanyl-sulfanylidene-$l^{5}-phosphane Chemical compound [NH4+].COP([S-])(=S)OC PPGORMGERPBFTJ-UHFFFAOYSA-N 0.000 description 1
230000001580 bacterial effect Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Chemical group 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
239000003093 cationic surfactant Substances 0.000 description 1
229910052570 clay Inorganic materials 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000013256 coordination polymer Substances 0.000 description 1
IRDLUHRVLVEUHA-UHFFFAOYSA-N diethyl dithiophosphate Chemical compound CCOP(S)(=S)OCC IRDLUHRVLVEUHA-UHFFFAOYSA-N 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
235000013305 food Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
239000001963 growth medium Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000008263 liquid aerosol Substances 0.000 description 1
230000003211 malignant effect Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
239000002609 medium Substances 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
150000002898 organic sulfur compounds Chemical class 0.000 description 1
239000006072 paste Substances 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000003760 tallow Substances 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1
239000003440 toxic substance Substances 0.000 description 1
238000010396 two-hybrid screening Methods 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)

CS829028A 1981-12-10 1982-12-10 Insekticidni a nematocidni prostredek CS902882A2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US06/329,157 US4395551A (en)	1981-12-10	1981-12-10	Pyridopyrimidinone compounds

Publications (1)

Publication Number	Publication Date
CS902882A2 true CS902882A2 (en)	1985-07-16

Family

ID=23284113

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS829028A CS902882A2 (en)	1981-12-10	1982-12-10	Insekticidni a nematocidni prostredek

Country Status (21)

Country	Link
US (1)	US4395551A (es)
EP (3)	EP0091700A3 (es)
JP (1)	JPS6024116B2 (es)
KR (1)	KR840002847A (es)
AT (1)	ATE21906T1 (es)
AU (1)	AU9093382A (es)
BR (1)	BR8207071A (es)
CA (1)	CA1184911A (es)
CS (1)	CS902882A2 (es)
DD (1)	DD210835A5 (es)
DE (1)	DE3273062D1 (es)
DK (1)	DK546982A (es)
ES (2)	ES8405416A1 (es)
GR (1)	GR77085B (es)
IL (1)	IL67341A (es)
NO (1)	NO824109L (es)
PH (1)	PH19372A (es)
PL (1)	PL239429A1 (es)
PT (1)	PT75959B (es)
TR (1)	TR21566A (es)
ZA (1)	ZA828670B (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4634690A (en) *	1981-12-10	1987-01-06	Uniroyal Chemical Company, Inc.	Substituted pyrimidinyl organophosphorus insecticides
AU2278183A (en) *	1983-01-07	1984-07-12	F. Hoffmann-La Roche & Co.	Pyrimidine di thiophosphate derivatives

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3243437A (en) *	1957-10-25	1966-03-29	Ici Ltd	Pyrimidine phosphorothioates
BE788828A (fr) *	1971-09-16	1973-03-14	Roussel Uclaf	Nouveaux derives organophosphores heterocycliques et procede depreparation
FR2198697B1 (es) *	1972-09-11	1975-09-12	Roussel Uclaf
HU168541B (es) *	1973-11-24	1976-05-28
US3960863A (en) *	1974-06-25	1976-06-01	Sankyo Company Limited	Pyrido[1,2-a]pyrimidinone derivatives
DE2838359A1 (de) *	1978-09-02	1980-03-20	Bayer Ag	N,n-dimethyl-0-pyrimidinyl-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel
JPS55104295A (en) *	1979-02-05	1980-08-09	Sumitomo Chem Co Ltd	Pyrimidin-4-yl(thio)phosphoric acid ester, its preparation, and insecticide, miticide, and nematocide containing the compound as effective component
JPS55104294A (en) *	1979-02-05	1980-08-09	Sumitomo Chem Co Ltd	Thio- or dithiophosphoric acid ester, its preparation, and insecticide, miticide, and menatocide containing the compound as effective component

1981
- 1981-12-10 US US06/329,157 patent/US4395551A/en not_active Expired - Lifetime
1982
- 1982-11-19 CA CA000415950A patent/CA1184911A/en not_active Expired
- 1982-11-24 ZA ZA828670A patent/ZA828670B/xx unknown
- 1982-11-26 IL IL67341A patent/IL67341A/xx unknown
- 1982-11-26 AU AU90933/82A patent/AU9093382A/en not_active Abandoned
- 1982-12-01 DE DE8282306400T patent/DE3273062D1/de not_active Expired
- 1982-12-01 EP EP83106372A patent/EP0091700A3/en not_active Withdrawn
- 1982-12-01 AT AT82306400T patent/ATE21906T1/de not_active IP Right Cessation
- 1982-12-01 EP EP82306400A patent/EP0081945B1/en not_active Expired
- 1982-12-01 EP EP85100986A patent/EP0156121A2/en not_active Withdrawn
- 1982-12-03 TR TR21566A patent/TR21566A/xx unknown
- 1982-12-06 BR BR8207071A patent/BR8207071A/pt unknown
- 1982-12-07 NO NO824109A patent/NO824109L/no unknown
- 1982-12-08 KR KR1019820005499A patent/KR840002847A/ko unknown
- 1982-12-09 DK DK546982A patent/DK546982A/da not_active Application Discontinuation
- 1982-12-09 PT PT75959A patent/PT75959B/pt unknown
- 1982-12-09 DD DD82245786A patent/DD210835A5/de unknown
- 1982-12-09 PL PL23942982A patent/PL239429A1/xx unknown
- 1982-12-10 ES ES518087A patent/ES8405416A1/es not_active Expired
- 1982-12-10 PH PH28261A patent/PH19372A/en unknown
- 1982-12-10 JP JP57216776A patent/JPS6024116B2/ja not_active Expired
- 1982-12-10 GR GR70045A patent/GR77085B/el unknown
- 1982-12-10 CS CS829028A patent/CS902882A2/cs unknown
1984
- 1984-02-29 ES ES530167A patent/ES8505693A1/es not_active Expired

Also Published As

Publication number	Publication date
EP0081945B1 (en)	1986-09-03
PH19372A (en)	1986-04-02
TR21566A (tr)	1984-10-03
IL67341A0 (en)	1983-03-31
EP0091700A3 (en)	1984-04-25
BR8207071A (pt)	1983-10-11
PL239429A1 (en)	1983-09-12
ATE21906T1 (de)	1986-09-15
ES518087A0 (es)	1984-06-01
EP0156121A2 (en)	1985-10-02
IL67341A (en)	1986-07-31
JPS58126871A (ja)	1983-07-28
ES530167A0 (es)	1985-06-01
EP0081945A2 (en)	1983-06-22
US4395551A (en)	1983-07-26
DD210835A5 (de)	1984-06-27
NO824109L (no)	1983-06-13
JPS6024116B2 (ja)	1985-06-11
CA1184911A (en)	1985-04-02
GR77085B (es)	1984-09-06
AU9093382A (en)	1983-06-16
PT75959A (en)	1983-01-01
PT75959B (en)	1985-12-16
EP0091700A2 (en)	1983-10-19
DE3273062D1 (en)	1986-10-09
ES8405416A1 (es)	1984-06-01
ZA828670B (en)	1983-09-28
KR840002847A (ko)	1984-07-21
EP0081945A3 (en)	1983-08-24
ES8505693A1 (es)	1985-06-01
DK546982A (da)	1983-06-11

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IL96913A (en)	1995-11-27	Progeny history Intermediate materials for the preparation of Seelan history Pesticides
KR20150103096A (ko)	2015-09-09	N-(치환된)-5-플루오로-4-이미노-3-메틸-2-옥소-3,4-디히드로피리미딘-1(2h)-카르복실레이트 유도체
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HU180532B (en)	1983-03-28	Insecticide compositions containing thiasolyl-cinnamonic nitriles
CS902882A2 (en)	1985-07-16	Insekticidni a nematocidni prostredek
IL27678A (en)	1972-07-26	Pyrimidine containing phosphorus compounds and insecticidal and fungicidal compositions containing them
GB2043643A (en)	1980-10-08	Phosphorus containing pyrimidine compounds
JPS61145107A (ja)	1986-07-02	有機リン化合物の殺虫活性を向上するための方法および組成物
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GB2085878A (en)	1982-05-06	Insecticidal heterocyclic ether or thioether linkage containing urea compounds
CS199286B2 (en)	1980-07-31	Fungicides,insecticides,acaricides,nematocides and herbicides and method of producing active compounds
JPH05501550A (ja)	1993-03-25	ピリミジン誘導体、それらの製造方法、それらを含有する薬剤及びそれらを殺菌剤として使用する方法
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CN1060008A (zh)	1992-04-08	4-喹喔啉氧基苯氧基烷基腈类除草剂
JPH0248572A (ja)	1990-02-19	新規なチアゾール化合物及びその製造方法並びに該化合物を有効成分とする殺菌剤組成物
KR850001041B1 (ko)	1985-07-19	인산 및 포스폰산의 크산테논-일 에스테르의 제조방법
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EP0088484A1 (en)	1983-09-14	Herbicidal thiadiazolyl N-aminoureas
US4472389A (en)	1984-09-18	Substituted pyrimidinyl organophosphorus insecticides
US3551562A (en)	1970-12-29	Insecticidal use of s-((4-oxo-1,2,3-benzotriazin - 3(4h)-yl) - methyl) phosphorothioates and phosphorodithioates
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JPH0559015A (ja)	1993-03-09	ピリミジン誘導体及び該誘導体を有効成分とする除草剤
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