JPS5892665A - 置換ベンジルイミダゾリウム塩及び該化合物を含有する殺菌剤 - Google Patents

置換ベンジルイミダゾリウム塩及び該化合物を含有する殺菌剤

Info

Publication number: JPS5892665A
Authority: JP; Japan
Prior art keywords: group; atom; methyl; carbon atoms; alkyl
Prior art date: 1981-11-20
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.): Granted

Application number

JP19263782A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0375544B2 (fr

Inventor

トニ−・ドクナ−

エルンスト−ハインリヒ・ポマ−

マチアス・ヴエツラ−

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.)

BASF SE

Original Assignee

BASF SE

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.)

1981-11-20

Filing date

1982-11-04

Publication date

1983-06-02

1982-11-04 Application filed by BASF SE filed Critical BASF SE

1983-06-02 Publication of JPS5892665A publication Critical patent/JPS5892665A/ja

1991-12-02 Publication of JPH0375544B2 publication Critical patent/JPH0375544B2/ja

Status Granted legal-status Critical Current

Links

KKKDZZRICRFGSD-UHFFFAOYSA-O 3-benzyl-1h-imidazol-3-ium Chemical class C1=C[NH+]=CN1CC1=CC=CC=C1 KKKDZZRICRFGSD-UHFFFAOYSA-O 0.000 title claims description 3
239000000417 fungicide Chemical class 0.000 title description 4
230000000855 fungicidal effect Effects 0.000 title description 2
150000001875 compounds Chemical class 0.000 claims description 29
125000004429 atom Chemical group 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 13
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
229910052801 chlorine Inorganic materials 0.000 claims description 6
125000005843 halogen group Chemical group 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 5
125000001309 chloro group Chemical group Cl* 0.000 claims description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
239000000645 desinfectant Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims 7
239000013543 active substance Substances 0.000 description 15
239000000203 mixture Substances 0.000 description 10
-1 2-methyl-4-chloro-benzyl group Chemical group 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
238000004519 manufacturing process Methods 0.000 description 6
244000005700 microbiome Species 0.000 description 6
239000000243 solution Substances 0.000 description 6
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
241000894006 Bacteria Species 0.000 description 4
241000196324 Embryophyta Species 0.000 description 4
238000010790 dilution Methods 0.000 description 4
239000012895 dilution Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
241000233866 Fungi Species 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
238000004458 analytical method Methods 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000012467 final product Substances 0.000 description 3
230000012010 growth Effects 0.000 description 3
235000015097 nutrients Nutrition 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
241000195493 Cryptophyta Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
230000001580 bacterial effect Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
150000004962 phenylmethylimidazoles Chemical class 0.000 description 2
238000004321 preservation Methods 0.000 description 2
239000000047 product Substances 0.000 description 2
239000002994 raw material Substances 0.000 description 2
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
AOSZTAHDEDLTLQ-AZKQZHLXSA-N (1S,2S,4R,8S,9S,11S,12R,13S,19S)-6-[(3-chlorophenyl)methyl]-12,19-difluoro-11-hydroxy-8-(2-hydroxyacetyl)-9,13-dimethyl-6-azapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one Chemical compound C([C@@H]1C[C@H]2[C@H]3[C@]([C@]4(C=CC(=O)C=C4[C@@H](F)C3)C)(F)[C@@H](O)C[C@@]2([C@@]1(C1)C(=O)CO)C)N1CC1=CC=CC(Cl)=C1 AOSZTAHDEDLTLQ-AZKQZHLXSA-N 0.000 description 1
YQOLEILXOBUDMU-KRWDZBQOSA-N (4R)-5-[(6-bromo-3-methyl-2-pyrrolidin-1-ylquinoline-4-carbonyl)amino]-4-(2-chlorophenyl)pentanoic acid Chemical compound CC1=C(C2=C(C=CC(=C2)Br)N=C1N3CCCC3)C(=O)NC[C@H](CCC(=O)O)C4=CC=CC=C4Cl YQOLEILXOBUDMU-KRWDZBQOSA-N 0.000 description 1
IOQORVDNYPOZPL-VQTJNVASSA-N (5S,6R)-5-(4-chlorophenyl)-6-cyclopropyl-3-[6-methoxy-5-(4-methylimidazol-1-yl)pyridin-2-yl]-5,6-dihydro-2H-1,2,4-oxadiazine Chemical compound ClC1=CC=C(C=C1)[C@@H]1NC(=NO[C@@H]1C1CC1)C1=NC(=C(C=C1)N1C=NC(=C1)C)OC IOQORVDNYPOZPL-VQTJNVASSA-N 0.000 description 1
CSNIZNHTOVFARY-UHFFFAOYSA-N 1,2-benzothiazole Chemical compound C1=CC=C2C=NSC2=C1 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 description 1
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
IIGOMDAAKJTVTK-UHFFFAOYSA-N 1-dodecyl-5-iodo-4-methylimidazole Chemical compound CCCCCCCCCCCCN1C=NC(C)=C1I IIGOMDAAKJTVTK-UHFFFAOYSA-N 0.000 description 1
HLUVAKZYPQUXQC-UHFFFAOYSA-N 2,2,2-trihydroxyacetamide Chemical compound NC(=O)C(O)(O)O HLUVAKZYPQUXQC-UHFFFAOYSA-N 0.000 description 1
FQMZXMVHHKXGTM-UHFFFAOYSA-N 2-(1-adamantyl)-n-[2-[2-(2-hydroxyethylamino)ethylamino]quinolin-5-yl]acetamide Chemical compound C1C(C2)CC(C3)CC2CC13CC(=O)NC1=CC=CC2=NC(NCCNCCO)=CC=C21 FQMZXMVHHKXGTM-UHFFFAOYSA-N 0.000 description 1
OLQJQHSAWMFDJE-UHFFFAOYSA-N 2-(hydroxymethyl)-2-nitropropane-1,3-diol Chemical compound OCC(CO)(CO)[N+]([O-])=O OLQJQHSAWMFDJE-UHFFFAOYSA-N 0.000 description 1
WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 1
QDXAXXIPBMVWOH-UHFFFAOYSA-N 4-chloro-1-(chloromethyl)-2-methylbenzene Chemical compound CC1=CC(Cl)=CC=C1CCl QDXAXXIPBMVWOH-UHFFFAOYSA-N 0.000 description 1
QJHGJSHNFXKDQH-UHFFFAOYSA-N 4-chloro-5-methyl-1h-imidazole Chemical compound CC=1NC=NC=1Cl QJHGJSHNFXKDQH-UHFFFAOYSA-N 0.000 description 1
ZYGYULIGJXJLRW-UHFFFAOYSA-N 4-methyl-1h-indazole Chemical compound CC1=CC=CC2=C1C=NN2 ZYGYULIGJXJLRW-UHFFFAOYSA-N 0.000 description 1
KIQRXUUOCWDHHD-UHFFFAOYSA-N 5-chloro-1-decyl-4-methylimidazole Chemical compound CCCCCCCCCCN1C=NC(C)=C1Cl KIQRXUUOCWDHHD-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OAKZUWKCCHKBBZ-UHFFFAOYSA-N C(CCC)[Sn](CCCC)CCCC.C(SC#N)SC#N Chemical compound C(CCC)[Sn](CCCC)CCCC.C(SC#N)SC#N OAKZUWKCCHKBBZ-UHFFFAOYSA-N 0.000 description 1
241000222120 Candida <Saccharomycetales> Species 0.000 description 1
229940126657 Compound 17 Drugs 0.000 description 1
241000588724 Escherichia coli Species 0.000 description 1
240000002989 Euphorbia neriifolia Species 0.000 description 1
SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
101100523604 Mus musculus Rassf5 gene Proteins 0.000 description 1
241000191967 Staphylococcus aureus Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000005791 algae growth Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
238000003287 bathing Methods 0.000 description 1
JBIROUFYLSSYDX-UHFFFAOYSA-M benzododecinium chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 JBIROUFYLSSYDX-UHFFFAOYSA-M 0.000 description 1
KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
229940073608 benzyl chloride Drugs 0.000 description 1
230000000740 bleeding effect Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
210000001072 colon Anatomy 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
229940126540 compound 41 Drugs 0.000 description 1
229940125844 compound 46 Drugs 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000000921 elemental analysis Methods 0.000 description 1
210000000744 eyelid Anatomy 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
238000009434 installation Methods 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
239000000155 melt Substances 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
210000005239 tubule Anatomy 0.000 description 1
230000037303 wrinkles Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/68—Halogen 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles

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)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

JP19263782A 1981-11-20 1982-11-04 置換ベンジルイミダゾリウム塩及び該化合物を含有する殺菌剤 Granted JPS5892665A (ja)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE3145928.5		1981-11-20
DE19813145927 DE3145927A1 (de)	1981-11-20	1981-11-20	4(5)-methyl-5(4)-chlorimidazol und verfahren zu seiner herstellung
DE3145927.7		1981-11-20

Publications (2)

Publication Number	Publication Date
JPS5892665A true JPS5892665A (ja)	1983-06-02
JPH0375544B2 JPH0375544B2 (fr)	1991-12-02

Family

ID=6146749

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP19263782A Granted JPS5892665A (ja)	1981-11-20	1982-11-04	置換ベンジルイミダゾリウム塩及び該化合物を含有する殺菌剤

Country Status (2)

Country	Link
JP (1)	JPS5892665A (fr)
DE (1)	DE3145927A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2008031100A (ja) *	2006-07-28	2008-02-14	Japan Enviro Chemicals Ltd	工業用殺菌剤およびそれを用いた殺菌方法

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ES2108894T3 (es) *	1993-03-12	1998-01-01	Lonza Ag	Procedimiento para la preparacion de 5-cloroimidazoles eventualmente sustituidos en posicion 2.
US5484939A (en) *	1993-03-12	1996-01-16	Lonza Ltd.	2-substituted 5-chlorimidazoles

1981
- 1981-11-20 DE DE19813145927 patent/DE3145927A1/de not_active Withdrawn
1982
- 1982-11-04 JP JP19263782A patent/JPS5892665A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2008031100A (ja) *	2006-07-28	2008-02-14	Japan Enviro Chemicals Ltd	工業用殺菌剤およびそれを用いた殺菌方法

Also Published As

Publication number	Publication date
JPH0375544B2 (fr)	1991-12-02
DE3145927A1 (de)	1983-06-01

Publication	Publication Date	Title
JPS6042202B2 (ja)	1985-09-20	植物真菌防除剤及びその製法
PL110714B1 (en)	1980-07-31	Method of producing new heterocyclic derivatives containing in ring nitrogen,specially oxazolidine or thiazolidine
JPH02180848A (ja)	1990-07-13	抗微生物化合物
JPS6011691B2 (ja)	1985-03-27	抗菌及び殺菌剤
DE1693052A1 (de)	1971-05-13	Schaedlingsbekaempfungsmittel
JPH01305064A (ja)	1989-12-08	２―フエニルスルフイニル―ニトロ―ピリジン類
JPS5892665A (ja)	1983-06-02	置換ベンジルイミダゾリウム塩及び該化合物を含有する殺菌剤
JPH01221371A (ja)	1989-09-04	環状オキシアミン誘導体の製造方法
JPS59116203A (ja)	1984-07-05	ピロ−ル誘導体を含有する殺菌剤
CA1181082A (fr)	1985-01-15	Sels de benzylimidazolium substitues et microbicides renfermant ces composes
JPS62281886A (ja)	1987-12-07	フオスフアイト誘導体及びその製造方法
US5552423A (en)	1996-09-03	Isothiazolone derivative and microbicidal composition comprising the same as active ingredient
US4199581A (en)	1980-04-22	1,4-Dithiino pyrazine tetracarbonitriles
US4209522A (en)	1980-06-24	Antimicrobial bis(5-nitro-2-thiazolyl)thioisothiazoles and thiadiazoles
US4147784A (en)	1979-04-03	4,5-Dihydro-4-oxo-1,3-dithiolo(4,5-D)pyridazine-2-ylidene-propanedinitriles
US4148899A (en)	1979-04-10	((5-Nitro-2-thiazolyl)thio)polyhalogenated pyridines
US4183957A (en)	1980-01-15	N'-(substituted phenyl)-N-(2-(halophenoxy)ethyl)alkylanimidamides
CA1189517A (fr)	1985-06-25	Sels de benzylimidazolium substitues et microbicides les contenant
JPH04290865A (ja)	1992-10-15	殺虫性、殺ダニ性ジアリールピロールカーボニトリルとジアリールニトロピロール化合物
US3355352A (en)	1967-11-28	Fungicidal composition
US3031373A (en)	1962-04-24	8-quinolyl carbonate derivatives
DE3145928A1 (de)	1983-06-01	Substituierte benzylimidazoliumsalzue und diese enthaltende mikrozide
CH398615A (de)	1966-03-15	Verfahren zur Herstellung von neuen quaternären Piperaziniumverbindungen
DE68905202T2 (de)	1993-09-16	Imidazolderivate, verfahren zu ihrer herstellung und sie enthaltende fungizide zusammensetzungen zu landwirtschaftlichen und gartenbau-verwendungen.
JPS62270508A (ja)	1987-11-24	殺生物剤組成物

JPS5892665A - 置換ベンジルイミダゾリウム塩及び該化合物を含有する殺菌剤 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (3)

Publications (2)

Family

ID=6146749

Family Applications (1)

Country Status (2)

Cited By (1)

Families Citing this family (2)

Cited By (1)

Also Published As

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