JPS59205304A - 殺菌・殺カビ剤類 - Google Patents

殺菌・殺カビ剤類

Info

Publication number: JPS59205304A
Authority: JP; Japan
Prior art keywords: butyl; formula; thiadiazol; alkyl; substituted
Prior art date: 1983-04-19
Legal status (The legal status 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 status listed.): Pending

Application number

JP59075900A

Other languages

English (en)

Japanese (ja)

Inventor

ビンフリ−ト・ルンケンハイマ−

パウル・ライネツケ

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

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.)

1983-04-19

Filing date

1984-04-17

Publication date

1984-11-20

1984-04-17 Application filed by Bayer AG filed Critical Bayer AG

1984-11-20 Publication of JPS59205304A publication Critical patent/JPS59205304A/ja

Status Pending legal-status Critical Current

Links

239000000417 fungicide Substances 0.000 title claims description 12
230000000844 anti-bacterial effect Effects 0.000 title claims description 6
235000013339 cereals Nutrition 0.000 claims description 13
230000000855 fungicidal effect Effects 0.000 claims description 13
201000010099 disease Diseases 0.000 claims description 12
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 11
229910052739 hydrogen Inorganic materials 0.000 claims description 10
229910052731 fluorine Inorganic materials 0.000 claims description 9
239000001257 hydrogen Substances 0.000 claims description 9
229910052736 halogen Inorganic materials 0.000 claims description 8
150000002367 halogens Chemical group 0.000 claims description 8
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 7
125000004432 carbon atom Chemical group C* 0.000 claims description 7
239000000460 chlorine Substances 0.000 claims description 7
229910052801 chlorine Inorganic materials 0.000 claims description 7
239000011737 fluorine Substances 0.000 claims description 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
229910052794 bromium Inorganic materials 0.000 claims description 5
241000233866 Fungi Species 0.000 claims description 4
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
239000004606 Fillers/Extenders Substances 0.000 claims description 3
239000003899 bactericide agent Substances 0.000 claims description 3
244000053095 fungal pathogen Species 0.000 claims description 3
125000001188 haloalkyl group Chemical group 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 2
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 2
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
238000002156 mixing Methods 0.000 claims description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
239000004094 surface-active agent Substances 0.000 claims description 2
239000004202 carbamide Substances 0.000 claims 2
235000013877 carbamide Nutrition 0.000 claims 2
HQECKTIAEXKUOS-UHFFFAOYSA-N (5-tert-butyl-1,3,4-thiadiazol-2-yl)urea Chemical class CC(C)(C)C1=NN=C(NC(N)=O)S1 HQECKTIAEXKUOS-UHFFFAOYSA-N 0.000 claims 1
UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 claims 1
125000006519 CCH3 Chemical group 0.000 claims 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
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XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
238000009472 formulation Methods 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000008187 granular material Substances 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 5
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ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
238000000889 atomisation Methods 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
239000012990 dithiocarbamate Substances 0.000 description 3
238000003958 fumigation Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
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238000012360 testing method Methods 0.000 description 3
239000011701 zinc Substances 0.000 description 3
229910052725 zinc Inorganic materials 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
239000004604 Blowing Agent Substances 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
241001503460 Plasmodiophorida Species 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
241000221300 Puccinia Species 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
241000209140 Triticum Species 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
125000002877 alkyl aryl group Chemical group 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 2
238000000576 coating method Methods 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000975 dye Substances 0.000 description 2
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150000002170 ethers Chemical class 0.000 description 2
239000004009 herbicide Substances 0.000 description 2
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239000002917 insecticide Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
239000003595 mist Substances 0.000 description 2
XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
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235000009566 rice Nutrition 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000002002 slurry Substances 0.000 description 2
QUKGLNCXGVWCJX-UHFFFAOYSA-N 1,3,4-thiadiazol-2-amine Chemical class NC1=NN=CS1 QUKGLNCXGVWCJX-UHFFFAOYSA-N 0.000 description 1
229940057054 1,3-dimethylurea Drugs 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
RPFXMKLCYJSYDE-UHFFFAOYSA-N 3-fluoropropanoic acid Chemical compound OC(=O)CCF RPFXMKLCYJSYDE-UHFFFAOYSA-N 0.000 description 1
JHVZDULURDIGDW-UHFFFAOYSA-N 4-fluoro-3,3-dimethylbutan-2-one Chemical compound CC(=O)C(C)(C)CF JHVZDULURDIGDW-UHFFFAOYSA-N 0.000 description 1
PTVZQOAHCSKAAS-UHFFFAOYSA-N 4-methyl-3-thiosemicarbazide Chemical compound CNC(=S)NN PTVZQOAHCSKAAS-UHFFFAOYSA-N 0.000 description 1
IIAQTAYBXGFHHT-UHFFFAOYSA-N 5-(1-fluoro-2-methylpropan-2-yl)-n-methyl-1,3,4-thiadiazol-2-amine Chemical compound CNC1=NN=C(C(C)(C)CF)S1 IIAQTAYBXGFHHT-UHFFFAOYSA-N 0.000 description 1
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RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
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150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
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239000008199 coating composition Substances 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
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GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
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WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
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IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
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229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
230000003389 potentiating effect Effects 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
229960003351 prussian blue Drugs 0.000 description 1
239000013225 prussian blue Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000011435 rock Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
235000010262 sodium metabisulphite Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000008096 xylene Substances 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
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
- C07D285/135—Nitrogen atoms
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof

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)
Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Plural Heterocyclic Compounds (AREA)

JP59075900A 1983-04-19 1984-04-17 殺菌・殺カビ剤類 Pending JPS59205304A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE33141908		1983-04-19
DE19833314190 DE3314190A1 (de)	1983-04-19	1983-04-19	Fungizide mittel

Publications (1)

Publication Number	Publication Date
JPS59205304A true JPS59205304A (ja)	1984-11-20

Family

ID=6196802

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP59075900A Pending JPS59205304A (ja)	1983-04-19	1984-04-17	殺菌・殺カビ剤類

Country Status (12)

Country	Link
JP (1)	JPS59205304A (da)
AU (1)	AU2680884A (da)
BE (1)	BE899439A (da)
BR (1)	BR8401819A (da)
DE (1)	DE3314190A1 (da)
DK (1)	DK203184A (da)
FR (1)	FR2544587A1 (da)
GB (1)	GB2138684A (da)
IT (1)	IT1209529B (da)
NL (1)	NL8401161A (da)
SE (1)	SE8401989L (da)
ZA (1)	ZA842914B (da)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN102276552B (zh) *	2011-06-15	2013-07-10	中国农业大学	含环丙烷基的1,3,4-噻二唑啉衍生物及其制备方法与作为杀菌剂的应用
CN117603160A (zh) *	2023-12-28	2024-02-27	山东华阳农药化工集团有限公司	一种高纯度特丁噻草隆的合成方法

1983
- 1983-04-19 DE DE19833314190 patent/DE3314190A1/de not_active Withdrawn
1984
- 1984-04-10 SE SE8401989A patent/SE8401989L/xx not_active Application Discontinuation
- 1984-04-11 NL NL8401161A patent/NL8401161A/nl not_active Application Discontinuation
- 1984-04-13 AU AU26808/84A patent/AU2680884A/en not_active Abandoned
- 1984-04-17 BE BE0/212778A patent/BE899439A/fr not_active IP Right Cessation
- 1984-04-17 JP JP59075900A patent/JPS59205304A/ja active Pending
- 1984-04-18 ZA ZA842914A patent/ZA842914B/xx unknown
- 1984-04-18 DK DK203184A patent/DK203184A/da not_active Application Discontinuation
- 1984-04-18 IT IT8420605A patent/IT1209529B/it active
- 1984-04-18 BR BR8401819A patent/BR8401819A/pt unknown
- 1984-04-18 FR FR8406110A patent/FR2544587A1/fr not_active Withdrawn
- 1984-04-18 GB GB08410103A patent/GB2138684A/en not_active Withdrawn

Also Published As

Publication number	Publication date
DK203184D0 (da)	1984-04-18
SE8401989D0 (sv)	1984-04-10
DK203184A (da)	1984-10-20
DE3314190A1 (de)	1984-10-25
IT8420605A0 (it)	1984-04-18
AU2680884A (en)	1984-10-25
IT1209529B (it)	1989-08-30
BE899439A (fr)	1984-10-17
NL8401161A (nl)	1984-11-16
FR2544587A1 (fr)	1984-10-26
GB8410103D0 (en)	1984-05-31
BR8401819A (pt)	1984-11-27
SE8401989L (sv)	1984-10-20
GB2138684A (en)	1984-10-31
ZA842914B (en)	1984-12-24

Publication	Publication Date	Title
US4042372A (en)	1977-08-16	Substituted thiadiazolotriazinediones and method of preparation
MXPA01007923A (es)	2002-10-01	Derivados de n2-fenil-amidina.
IE46260B1 (en)	1983-04-20	N-(azolylmethyl)-haloacetanilides and their use as herbicides
JPS63162680A (ja)	1988-07-06	オキサジアゾール誘導体およびそれを含む有害生物防除剤組成物
US4174398A (en)	1979-11-13	Combating fungi with 1-alkyl-1-(1,3,4-thiadiazol-2-yl)-3-phenyl-ureas
JPS5823673A (ja)	1983-02-12	新規なイミダゾリル誘導体およびその塩の製法
WO1992007835A1 (en)	1992-05-14	Imidazole fungicides
CS202519B2 (en)	1981-01-30	Fungicide and bactericide means for fighting the plant diseases
IL44821A (en)	1977-07-31	Plant fungicidal and mircobicidal compositions containing certaining certain omega-imidazolyl-omega-phenoxy(or phenylthio)-alkanones
US4146646A (en)	1979-03-27	Bis-amide fungicidal compounds
JPS59112904A (ja)	1984-06-29	殺菌剤
JPS6222763A (ja)	1987-01-30	新規なｎ−（２−フルオロフエニル）−アゾリジン及びその製造方法、並びに除草及び植物生長調節用組成物
JPS58967A (ja)	1983-01-06	菌・カビ防除組成物
US5096915A (en)	1992-03-17	Azole fungicides
CS270566B2 (en)	1990-07-12	Fungicide and method of its active substance production
JPS6087269A (ja)	1985-05-16	１‐アゾリル‐置換されたオキシムエーテル類
JPS59205304A (ja)	1984-11-20	殺菌・殺カビ剤類
JPS5855481A (ja)	1983-04-01	ヘテロ−置換されたピリド−４−オン誘導体類、それらの製造方法及び除草剤としてのそれらの使用
JPS5896073A (ja)	1983-06-07	アゾリルビニルジチオアセタ−ル類、それらの製造法および殺菌剤としての用途
HU191495B (en)	1987-02-27	Fungicides containing as active substance derivatives of hydroxi-alkinil-azol and process for production of the active substance
JPS63258878A (ja)	1988-10-26	殺線虫組成物
DE2853196A1 (de)	1980-06-26	1,3,4-thiadiazol-2-carbonsaeure-derivate, verfahren zur herstellung dieser verbindungen sowie diese enthaltende fungizide und nematizide mittel
JPS58213758A (ja)	1983-12-12	ヘテロアリ−ルチオビニル化合物、その製造法およびその農薬としての使用
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
US4405743A (en)	1983-09-20	Pyrazolylpyrimidine derivatives