BE897119A - Derives de 1,2,4-triadiazole - Google Patents

Derives de 1,2,4-triadiazole Download PDF

Info

Publication number: BE897119A
Authority: BE; Belgium
Prior art keywords: sep; group; carbon atoms; group containing; alkylthio
Prior art date: 1982-06-24

Application number

BE0/211056A

Other languages

English (en)

French (fr)

Inventor

K Hagiwara

K Ishimitsu

S Hashimoto

S Shimoda

Original Assignee

Nippon Soda Co

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.)

1982-06-24

Filing date

1983-06-23

Publication date

1983-10-17

1983-06-23 Application filed by Nippon Soda Co filed Critical Nippon Soda Co

1983-10-17 Publication of BE897119A publication Critical patent/BE897119A/fr

Links

125000004432 carbon atom Chemical group C* 0.000 claims description 60
150000001875 compounds Chemical class 0.000 claims description 43
239000000203 mixture Substances 0.000 claims description 18
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 16
125000000217 alkyl group Chemical group 0.000 claims description 14
230000000855 fungicidal effect Effects 0.000 claims description 13
125000005843 halogen group Chemical group 0.000 claims description 13
-1 N-methylanilino group Chemical group 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
125000004414 alkyl thio group Chemical group 0.000 claims description 8
125000001188 haloalkyl group Chemical group 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 6
125000004663 dialkyl amino group Chemical group 0.000 claims description 6
YGTAZGSLCXNBQL-UHFFFAOYSA-N 1,2,4-thiadiazole Chemical class C=1N=CSN=1 YGTAZGSLCXNBQL-UHFFFAOYSA-N 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
125000005108 alkenylthio group Chemical group 0.000 claims description 3
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 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 3
125000000753 cycloalkyl group Chemical group 0.000 claims description 3
125000002541 furyl group Chemical group 0.000 claims description 3
125000004438 haloalkoxy group Chemical group 0.000 claims description 3
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
125000004660 phenylalkylthio group Chemical group 0.000 claims description 3
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
125000001544 thienyl group Chemical group 0.000 claims description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 22
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FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
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RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 2
MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 2
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XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 description 2
239000012442 inert solvent Substances 0.000 description 2
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239000002904 solvent Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
239000008096 xylene Substances 0.000 description 2
ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
FHNKBSDJERHDHZ-UHFFFAOYSA-N (2,4-dimethylphenyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=C(C)C=C1C FHNKBSDJERHDHZ-UHFFFAOYSA-N 0.000 description 1
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 description 1
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DPWOISJOHBVMNF-UHFFFAOYSA-N 2,3-dihydrothiadiazole Chemical compound N1NC=CS1 DPWOISJOHBVMNF-UHFFFAOYSA-N 0.000 description 1
YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 description 1
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QSNSCYSYFYORTR-UHFFFAOYSA-N 4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 description 1
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150000007529 inorganic bases Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
230000002262 irrigation Effects 0.000 description 1
238000003973 irrigation Methods 0.000 description 1
238000002955 isolation Methods 0.000 description 1
UFHLMYOGRXOCSL-UHFFFAOYSA-N isoprothiolane Chemical compound CC(C)OC(=O)C(C(=O)OC(C)C)=C1SCCS1 UFHLMYOGRXOCSL-UHFFFAOYSA-N 0.000 description 1
PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000006194 liquid suspension Substances 0.000 description 1
239000010721 machine oil Substances 0.000 description 1
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
229920000940 maneb Polymers 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 description 1
LCGLNKUTAGEVQW-UHFFFAOYSA-N methyl monoether Natural products COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
229960001952 metrifonate Drugs 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
230000002969 morbid Effects 0.000 description 1
KFVKPSOJAAJVSR-UHFFFAOYSA-N n-methylbenzenecarboximidoyl chloride Chemical compound CN=C(Cl)C1=CC=CC=C1 KFVKPSOJAAJVSR-UHFFFAOYSA-N 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 description 1
VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 1
LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
229960000490 permethrin Drugs 0.000 description 1
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
XAMUDJHXFNRLCY-UHFFFAOYSA-N phenthoate Chemical compound CCOC(=O)C(SP(=S)(OC)OC)C1=CC=CC=C1 XAMUDJHXFNRLCY-UHFFFAOYSA-N 0.000 description 1
LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 description 1
YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 description 1
YRRBXJLFCBCKNW-UHFFFAOYSA-N prothiocarb Chemical compound CCSC(=O)NCCCN(C)C YRRBXJLFCBCKNW-UHFFFAOYSA-N 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
VEMKTZHHVJILDY-UHFFFAOYSA-N resmethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UHFFFAOYSA-N 0.000 description 1
239000013049 sediment Substances 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
DVQHRBFGRZHMSR-UHFFFAOYSA-N sodium methyl 2,2-dimethyl-4,6-dioxo-5-(N-prop-2-enoxy-C-propylcarbonimidoyl)cyclohexane-1-carboxylate Chemical compound [Na+].C=CCON=C(CCC)[C-]1C(=O)CC(C)(C)C(C(=O)OC)C1=O DVQHRBFGRZHMSR-UHFFFAOYSA-N 0.000 description 1
VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 description 1
CXBMCYHAMVGWJQ-UHFFFAOYSA-N tetramethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-UHFFFAOYSA-N 0.000 description 1
OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/08—1,2,4-Thiadiazoles; Hydrogenated 1,2,4-thiadiazoles
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)

BE0/211056A 1982-06-24 1983-06-23 Derives de 1,2,4-triadiazole BE897119A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP57108884A JPS58225077A (ja)	1982-06-24	1982-06-24	１，２，４−チアジアゾ−ル誘導体及び農園芸用殺菌剤

Publications (1)

Publication Number	Publication Date
BE897119A true BE897119A (fr)	1983-10-17

Family

ID=14496031

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE0/211056A BE897119A (fr)	1982-06-24	1983-06-23	Derives de 1,2,4-triadiazole

Country Status (12)

Country	Link
JP (1)	JPS58225077A (de)
KR (1)	KR840005119A (de)
BE (1)	BE897119A (de)
CH (1)	CH654835A5 (de)
DE (1)	DE3322662A1 (de)
ES (1)	ES8500922A1 (de)
FR (1)	FR2529204A1 (de)
GB (1)	GB2124212B (de)
HU (1)	HU193169B (de)
IL (1)	IL69021A (de)
IT (1)	IT1174762B (de)
NL (1)	NL8302260A (de)

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3260725A (en) *	1961-03-15	1966-07-12	Olin Mathieson	3-trichloromethyl-5-substituted-1, 2, 4-thiadiazole
US3324141A (en) *	1965-08-12	1967-06-06	Olin Mathieson	3-trichloromethyl-5-amino-1, 2, 4-thiadiazoles
US3574226A (en) *	1967-05-19	1971-04-06	Ansul Co	Substituted delta**2-1,2,4-thiadiazolin-5-ones
DE1907116A1 (de) *	1969-02-13	1970-09-03	Bayer Ag	5-Chlor-3-oxo-1,2,4-thiadiazoline
DE1925995A1 (de) *	1969-05-21	1970-11-26	Bayer Ag	2-Alkyloxymethyl-3-chlor-1,2,4-thiaimidazol-5-one
US3764685A (en) *	1970-09-08	1973-10-09	Velsicol Chemical Corp	Certain thiadiazoles as fungicides
US3884929A (en) *	1970-12-14	1975-05-20	Eric Smith	Selected 3-trichloromethyl-5-substituted 1,2,4-thiadiazoles
BE788149A (fr) *	1971-08-31	1973-02-28	Ciba Geigy	Application de derives du thiadiazole a la conservation de nourritures pour animaux

1982
- 1982-06-24 JP JP57108884A patent/JPS58225077A/ja active Granted
1983
- 1983-06-17 IL IL69021A patent/IL69021A/xx unknown
- 1983-06-23 HU HU832231A patent/HU193169B/hu unknown
- 1983-06-23 DE DE19833322662 patent/DE3322662A1/de not_active Withdrawn
- 1983-06-23 IT IT48572/83A patent/IT1174762B/it active
- 1983-06-23 KR KR1019830002824A patent/KR840005119A/ko not_active Abandoned
- 1983-06-23 GB GB08317065A patent/GB2124212B/en not_active Expired
- 1983-06-23 ES ES523567A patent/ES8500922A1/es not_active Expired
- 1983-06-23 BE BE0/211056A patent/BE897119A/fr not_active IP Right Cessation
- 1983-06-23 FR FR8310414A patent/FR2529204A1/fr active Granted
- 1983-06-24 CH CH3474/83A patent/CH654835A5/de not_active IP Right Cessation
- 1983-06-24 NL NL8302260A patent/NL8302260A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
ES523567A0 (es)	1984-11-01
NL8302260A (nl)	1984-01-16
IT8348572A0 (it)	1983-06-23
JPS58225077A (ja)	1983-12-27
FR2529204A1 (fr)	1983-12-30
GB2124212B (en)	1985-10-09
GB8317065D0 (en)	1983-07-27
IL69021A (en)	1986-09-30
HU193169B (en)	1987-08-28
GB2124212A (en)	1984-02-15
CH654835A5 (de)	1986-03-14
DE3322662A1 (de)	1983-12-29
IL69021A0 (en)	1983-10-31
FR2529204B1 (de)	1985-05-17
KR840005119A (ko)	1984-11-03
JPH038347B2 (de)	1991-02-05
ES8500922A1 (es)	1984-11-01
IT1174762B (it)	1987-07-01

Legal Events

Date

Code

Title

Description

1988-12-31

RE

Patent lapsed

Owner name: NIPPON SODA CY LTD

Effective date: 19880630

Publication	Publication Date	Title
EP0402246B1 (de)	1994-08-24	Thiazolylalkoxyakrylate, ihre Herstellung, ihre Verwendung als Fungizide und Zwischenprodukte bei ihrer Herstellung
AU658955B2 (en)	1995-05-04	An oxazoline derivative, its production and its use
FR2597866A1 (fr)	1987-10-30	Derives du pyrazole, procede de preparation de ceux-ci et fongicide les contenant.
EP0245989B1 (de)	1991-07-10	Fluorphthalimide
FR2667316A1 (fr)	1992-04-03	Nouveaux derives du benzofuranne, leur procede de preparation et leur application comme pesticides.
US5371106A (en)	1994-12-06	3,4-diaryl-5(H)-furan-2-one based compounds with fungicidal activity
US4353916A (en)	1982-10-12	Benzothiazol-2-ones and phytopathogenic fungicidal use thereof
EP0265305B1 (de)	1991-06-12	5-Pyrazolon-Derivate, Verfahren zu deren Herstellung, deren Anwendung als Herbizide und deren Zusammensetzungen
FR2582647A1 (fr)	1986-12-05	Derives du phenanthrene, leur procede de preparation et compositions fongicides les contenant
FR2495609A1 (fr)	1982-06-11	Acylurees, procedes pour les preparer et produits insecticides contenant de tels composes
EP0239508A2 (de)	1987-09-30	2-Cyano-benzimidazol-Derivate, Verfahren zu deren Herstellung und Anwendung als Fungizide, deren Assoziation mit anderen Fungiziden
BE897119A (fr)	1983-10-17	Derives de 1,2,4-triadiazole
JP2503547B2 (ja)	1996-06-05	カルバモイルトリアゾ―ル誘導体、その製造法およびそれを有効成分とする除草剤
FR2513998A1 (fr)	1983-04-08	Composes fongicides
CH659249A5 (fr)	1987-01-15	Derives triazolyles et leur utilisation fongicide dans la domaine agricole.
BE886127A (fr)	1981-05-13	Nouveaux derives de l'imidazole, leur preparation et leur application comme agents fongicides
FR2476075A1 (fr)	1981-08-21	Nouveaux derives de l'acide methylene-2 succinamique, leur preparation et les compositions regulatrices de la croissance des plantes les contenant
EP0123931A2 (de)	1984-11-07	Furan-Derivate mit fungiziden Eigenschaften
JPS59222489A (ja)	1984-12-14	置換テトラヒドロチオピラン−３，５−ジオン−４−カルボキシアミド類
FR2462430A1 (fr)	1981-02-13	Nouvelles 1,2,4-triazolidine-3,5-dithiones trisubstituees en positions 1, 2 et 4, composition les contenant et leur utilisation comme herbicides et comme substances de croissance des plantes
JPH0655705B2 (ja)	1994-07-27	アシルアミノバレロニトリル誘導体、その製造法およびそれらを含有する除草剤および農園芸用殺菌剤
BE896914A (fr)	1983-12-01	Derives triazolyles et leur applecation fongicide
KR100477892B1 (ko)	2005-03-18	제초활성을 갖는9-(5-이속사졸메톡시페닐)이미노-8-치아-1,6-디아자비시클로[4.3.0]노난-7-온 유도체
CH637950A5 (fr)	1983-08-31	Derive de phenyl-2 dihydro-5,6 pyrone-4.
FR2512023A1 (fr)	1983-03-04	5-phenoxyphenyltetrahydro-1,3,5-thiadiazine-4-ones, leur preparation et leur utilisation dans la lutte contre les parasites