NO136733B - - Google Patents

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Info

Publication number: NO136733B
Authority: NO; Norway
Prior art keywords: methyl; thiazolone; carboxylic acid; ester; ethyl ester
Prior art date: 1972-10-28

Application number

NO4149/73A

Other languages

English (en)

Norwegian (no)

Inventor

K Grohe

P-E Frohberger

Original Assignee

Bayer Ag

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.)

1972-10-28

Filing date

1973-10-26

Publication date

1977-07-25

1973-10-26 Application filed by Bayer Ag filed Critical Bayer Ag

1977-07-25 Publication of NO136733B publication Critical patent/NO136733B/no

Links

125000000217 alkyl group Chemical group 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 5
239000000417 fungicide Substances 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 3
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
CZWWCTHQXBMHDA-UHFFFAOYSA-N 3h-1,3-thiazol-2-one Chemical compound OC1=NC=CS1 CZWWCTHQXBMHDA-UHFFFAOYSA-N 0.000 claims 1
239000004480 active ingredient Substances 0.000 claims 1
125000004188 dichlorophenyl group Chemical group 0.000 claims 1
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
239000013543 active substance Substances 0.000 description 23
-1 acyl acetic acid esters Chemical class 0.000 description 11
239000002253 acid Substances 0.000 description 7
238000005554 pickling Methods 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
241000196324 Embryophyta Species 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
241000209140 Triticum Species 0.000 description 6
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
239000000203 mixture Substances 0.000 description 6
MNOALXGAYUJNKX-UHFFFAOYSA-N s-chloro chloromethanethioate Chemical compound ClSC(Cl)=O MNOALXGAYUJNKX-UHFFFAOYSA-N 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000000126 substance Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
235000021307 Triticum Nutrition 0.000 description 5
GCFAUZGWPDYAJN-UHFFFAOYSA-N cyclohexyl 3-phenylprop-2-enoate Chemical compound C=1C=CC=CC=1C=CC(=O)OC1CCCCC1 GCFAUZGWPDYAJN-UHFFFAOYSA-N 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
230000000855 fungicidal effect Effects 0.000 description 5
239000007788 liquid Substances 0.000 description 5
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000002689 soil Substances 0.000 description 5
UKVYVZLTGQVOPX-NSCUHMNNSA-N (e)-3-aminobut-2-enoic acid Chemical compound C\C(N)=C/C(O)=O UKVYVZLTGQVOPX-NSCUHMNNSA-N 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
241000233866 Fungi Species 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
125000004494 ethyl ester group Chemical group 0.000 description 4
238000009472 formulation Methods 0.000 description 4
239000000725 suspension Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
238000009835 boiling Methods 0.000 description 3
239000000969 carrier Substances 0.000 description 3
235000013339 cereals Nutrition 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000007789 gas Substances 0.000 description 3
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
239000000047 product Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
206010017533 Fungal infection Diseases 0.000 description 2
239000005909 Kieselgur Substances 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
229910021529 ammonia Inorganic materials 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000004927 clay Substances 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000012990 dithiocarbamate Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
235000013312 flour Nutrition 0.000 description 2
239000006260 foam Substances 0.000 description 2
230000002538 fungal effect Effects 0.000 description 2
208000024386 fungal infectious disease Diseases 0.000 description 2
230000002464 fungitoxic effect Effects 0.000 description 2
230000035784 germination Effects 0.000 description 2
239000008187 granular material Substances 0.000 description 2
229930195733 hydrocarbon Natural products 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
238000000034 method Methods 0.000 description 2
239000006072 paste Substances 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
239000000843 powder Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
150000003141 primary amines Chemical class 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
239000011435 rock Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
ZMEVDFFLOPFGCR-UHFFFAOYSA-N 4-methyl-3h-1,3-thiazol-2-one Chemical compound CC1=CSC(O)=N1 ZMEVDFFLOPFGCR-UHFFFAOYSA-N 0.000 description 1
QCVGEOXPDFCNHA-UHFFFAOYSA-N 5,5-dimethyl-2,4-dioxo-1,3-oxazolidine-3-carboxamide Chemical compound CC1(C)OC(=O)N(C(N)=O)C1=O QCVGEOXPDFCNHA-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
102000002322 Egg Proteins Human genes 0.000 description 1
108010000912 Egg Proteins Proteins 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
WRQNANDWMGAFTP-UHFFFAOYSA-N Methylacetoacetic acid Chemical compound COC(=O)CC(C)=O WRQNANDWMGAFTP-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
241001123569 Puccinia recondita Species 0.000 description 1
206010037888 Rash pustular Diseases 0.000 description 1
241000722093 Tilletia caries Species 0.000 description 1
DRUIESSIVFYOMK-UHFFFAOYSA-N Trichloroacetonitrile Chemical compound ClC(Cl)(Cl)C#N DRUIESSIVFYOMK-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000008272 agar Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000001273 butane Substances 0.000 description 1
YTIVTFGABIZHHX-UHFFFAOYSA-N butynedioic acid Chemical class OC(=O)C#CC(O)=O YTIVTFGABIZHHX-UHFFFAOYSA-N 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000007681 cardiovascular toxicity Effects 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
239000002361 compost Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000002826 coolant Substances 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000010410 dusting Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
235000014103 egg white Nutrition 0.000 description 1
210000000969 egg white Anatomy 0.000 description 1
239000003974 emollient agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
231100000162 fungitoxic Toxicity 0.000 description 1
239000011521 glass Substances 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000011534 incubation Methods 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000463 material Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
239000002362 mulch Substances 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000003921 oil Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
RYFZYYUIAZYQLC-UHFFFAOYSA-N perchloromethyl mercaptan Chemical compound ClSC(Cl)(Cl)Cl RYFZYYUIAZYQLC-UHFFFAOYSA-N 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical class OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
208000029561 pustule Diseases 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Thiazole And Isothizaole Compounds (AREA)
Plural Heterocyclic Compounds (AREA)

NO4149/73A 1972-10-28 1973-10-26 NO136733B (tr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2253027A DE2253027A1 (de)	1972-10-28	1972-10-28	Fungizide mittel

Publications (1)

Publication Number	Publication Date
NO136733B true NO136733B (tr)	1977-07-25

Family

ID=5860337

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO4149/73A NO136733B (tr)	1972-10-28	1973-10-26

Country Status (21)

Country	Link
US (1)	US3932436A (tr)
JP (1)	JPS4975727A (tr)
AU (1)	AU476522B2 (tr)
BE (1)	BE806555A (tr)
BR (1)	BR7308386D0 (tr)
CA (1)	CA1014854A (tr)
CH (1)	CH558139A (tr)
CS (1)	CS179432B2 (tr)
DD (1)	DD107378A5 (tr)
DE (1)	DE2253027A1 (tr)
DK (1)	DK133763C (tr)
FR (1)	FR2204353B1 (tr)
GB (1)	GB1427554A (tr)
IE (1)	IE38426B1 (tr)
IL (1)	IL43479A0 (tr)
IT (1)	IT999008B (tr)
LU (1)	LU68701A1 (tr)
NL (1)	NL7314704A (tr)
NO (1)	NO136733B (tr)
PL (1)	PL87004B1 (tr)
TR (1)	TR17515A (tr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2818504A1 (de)	1978-04-27	1979-11-08	Bayer Ag	Mittel zur regulierung des pflanzenwachstums
US6924276B2 (en)	2001-09-10	2005-08-02	Warner-Lambert Company	Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors
EP2247603B1 (en)	2008-02-12	2016-09-28	Dow AgroSciences LLC	Pesticidal compositions
US8815922B2 (en) *	2011-02-07	2014-08-26	Dow Agrosciences, Llc.	Pesticidal compositions and processes related thereto
UA115126C2 (uk)	2011-07-12	2017-09-25	ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі	Пестицидні композиції і способи, які їх стосуються

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2678929A (en) *	1950-10-19	1954-05-18	Abbott Lab	4-thiazolidone-2-n-caproic acid and salts and method of preparing
BE786914A (fr) *	1971-07-28	1973-01-29	Bayer Ag	Esters d'acides thiazolinonecarboxyliques-2 et leur procede de preparation

1972
- 1972-10-28 DE DE2253027A patent/DE2253027A1/de active Pending
1973
- 1973-10-22 DD DD174210*A patent/DD107378A5/xx unknown
- 1973-10-24 AU AU61769/73A patent/AU476522B2/en not_active Expired
- 1973-10-24 TR TR17515A patent/TR17515A/tr unknown
- 1973-10-25 IL IL43479A patent/IL43479A0/xx unknown
- 1973-10-25 NL NL7314704A patent/NL7314704A/xx unknown
- 1973-10-26 CA CA184,307A patent/CA1014854A/en not_active Expired
- 1973-10-26 CH CH1511973A patent/CH558139A/xx not_active IP Right Cessation
- 1973-10-26 NO NO4149/73A patent/NO136733B/no unknown
- 1973-10-26 LU LU68701A patent/LU68701A1/xx unknown
- 1973-10-26 IT IT30632/73A patent/IT999008B/it active
- 1973-10-26 FR FR7338308A patent/FR2204353B1/fr not_active Expired
- 1973-10-26 GB GB4993773A patent/GB1427554A/en not_active Expired
- 1973-10-26 DK DK581373A patent/DK133763C/da active
- 1973-10-26 BR BR8386/73A patent/BR7308386D0/pt unknown
- 1973-10-26 CS CS7300007393A patent/CS179432B2/cs unknown
- 1973-10-26 JP JP48120022A patent/JPS4975727A/ja active Pending
- 1973-10-26 BE BE137095A patent/BE806555A/xx unknown
- 1973-10-26 IE IE1933/73A patent/IE38426B1/xx unknown
- 1973-10-26 US US05/410,073 patent/US3932436A/en not_active Expired - Lifetime
- 1973-10-27 PL PL1973166147A patent/PL87004B1/pl unknown

Also Published As

Publication number	Publication date
IE38426B1 (en)	1978-03-15
IE38426L (en)	1974-04-28
FR2204353B1 (tr)	1977-05-27
AU6176973A (en)	1975-04-24
JPS4975727A (tr)	1974-07-22
BR7308386D0 (pt)	1974-08-15
BE806555A (fr)	1974-04-26
US3932436A (en)	1976-01-13
DD107378A5 (tr)	1974-08-05
DK133763B (da)	1976-07-19
CA1014854A (en)	1977-08-02
TR17515A (tr)	1975-07-23
DK133763C (da)	1976-12-06
FR2204353A1 (tr)	1974-05-24
LU68701A1 (tr)	1974-01-08
NL7314704A (tr)	1974-05-01
IL43479A0 (en)	1974-01-14
IT999008B (it)	1976-02-20
PL87004B1 (tr)	1976-06-30
AU476522B2 (en)	1976-09-23
CH558139A (de)	1975-01-31
GB1427554A (en)	1976-03-10
CS179432B2 (en)	1977-10-31
DE2253027A1 (de)	1974-05-09

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CA1077048A (en)	1980-05-06	Pyrazole derivatives
JP3347170B2 (ja)	2002-11-20	トリアゾロピリミジン誘導体
JPS6115877A (ja)	1986-01-23	Ｎ‐（２‐ニトロフエニル）‐２‐アミノピリミジン誘導体、その製造方法及び該化合物を含有する組成物
JPH0676394B2 (ja)	1994-09-28	１、３―チアゾール誘導体、それらの製造方法および殺虫組成物
NO140061B (no)	1979-03-19	Tetrahydro-1,3,5-triazin-2,6-dioner med herbicide egenskaper
US5134144A (en)	1992-07-28	Pesticidal 3-arylpyrimidinyl ethers and thioethers
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