CA1119605A - 1,3-bis-(trihalomethylsulfenyl)-imidazoline-2,4- diones - Google Patents

1,3-bis-(trihalomethylsulfenyl)-imidazoline-2,4- diones

Info

Publication number: CA1119605A
Authority: CA; Canada
Prior art keywords: bis; imidazoline; parts; dione; weight
Prior art date: 1979-03-20
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.): Expired

Application number

CA000323847A

Other languages

English (en)

Inventor

Costin Rentzea

Ernst-Heinrich Pommer

Celia J. Mappes

Bernd Zeeh

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.)

1979-03-20

Filing date

1979-03-20

Publication date

1982-03-09

1979-03-20 Application filed by BASF SE filed Critical BASF SE

1979-03-20 Priority to CA000323847A priority Critical patent/CA1119605A/fr

1982-03-09 Application granted granted Critical

1982-03-09 Publication of CA1119605A publication Critical patent/CA1119605A/fr

Status Expired legal-status Critical Current

Links

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125000000217 alkyl group Chemical group 0.000 claims abstract description 5
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ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 4
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241000233866 Fungi Species 0.000 claims description 12
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150000002391 heterocyclic compounds Chemical class 0.000 description 1
CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
DBBRJAWSDTYYBM-UHFFFAOYSA-N isocyanatocyclopropane Chemical compound O=C=NC1CC1 DBBRJAWSDTYYBM-UHFFFAOYSA-N 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
229920005610 lignin Polymers 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
WJZHMLNIAZSFDO-UHFFFAOYSA-N manganese zinc Chemical compound [Mn].[Zn] WJZHMLNIAZSFDO-UHFFFAOYSA-N 0.000 description 1
238000004519 manufacturing process Methods 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
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000002828 nitro derivatives Chemical class 0.000 description 1
239000003921 oil Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229960003540 oxyquinoline Drugs 0.000 description 1
239000003973 paint Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
230000003032 phytopathogenic effect Effects 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
AHIHJODVQGBOND-UHFFFAOYSA-M propan-2-yl carbonate Chemical compound CC(C)OC([O-])=O AHIHJODVQGBOND-UHFFFAOYSA-M 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-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
238000001665 trituration Methods 0.000 description 1
JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1

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Agricultural Chemicals And Associated Chemicals (AREA)

CA000323847A 1979-03-20 1979-03-20 1,3-bis-(trihalomethylsulfenyl)-imidazoline-2,4- diones Expired CA1119605A (fr)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
CA000323847A CA1119605A (fr)	1979-03-20	1979-03-20	1,3-bis-(trihalomethylsulfenyl)-imidazoline-2,4- diones

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA000323847A CA1119605A (fr)	1979-03-20	1979-03-20	1,3-bis-(trihalomethylsulfenyl)-imidazoline-2,4- diones

Publications (1)

Publication Number	Publication Date
CA1119605A true CA1119605A (fr)	1982-03-09

Family

ID=4113793

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000323847A Expired CA1119605A (fr)	1979-03-20	1979-03-20	1,3-bis-(trihalomethylsulfenyl)-imidazoline-2,4- diones

Country Status (1)

Country	Link
CA (1)	CA1119605A (fr)

1979
- 1979-03-20 CA CA000323847A patent/CA1119605A/fr not_active Expired

Legal Events

Date	Code	Title	Description
1999-03-09	MKEX	Expiry

Publication	Publication Date	Title
US3501578A (en)	1970-03-17	Fungicidal composition containing phenyl - mercaptomethane-sulfonamide and method of using the same
EP0078450B1 (fr)	1985-10-02	Dérivés de pyridazinone, leur procédé de préparation et leur utilisation comme fongicides
US4521412A (en)	1985-06-04	Pesticidal iodopropargylammonium salts
US4350701A (en)	1982-09-21	1-(Trihalomethyl-sulfenyl)-4-aryl-1,2,4-triazolin-5-ones, and process for controlling fungi
IE50386B1 (en)	1986-04-16	Isoxazolylcarboxyanilides,their preparation,their use for combating fungi,and fungicides containing them
US4198423A (en)	1980-04-15	1,3-Bis-(trihalomethylsulfenyl)-imidazoline-2,4-diones
EP0364396A1 (fr)	1990-04-18	Agents neumaticides et fungicides
US4804671A (en)	1989-02-14	1-(trihalomethylsulfenyl)-4-aryl-1,2,4-triazolin-5-ones and fungicides containing these compounds
EP0065723B1 (fr)	1984-09-12	2-Méthylnaphtylamides N-substituées, leur préparation et leur emploi comme fongicides
EP0061037A1 (fr)	1982-09-29	Fongicides à base de 1,2-oxazolylphosphates et l'utilisation de ces agents actifs pour combattre les champignons
IE51494B1 (en)	1987-01-07	N-disubstituted aniline derivatives,their preparation,their use as microbicides and agents for such use
US4551458A (en)	1985-11-05	Quinazolines and fungicidal compositions thereof
EP0093274B1 (fr)	1985-07-24	Composés organosilyliques et leur application comme fongicides
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
US4496575A (en)	1985-01-29	Fungicidal N-sulphenylated hydantoins
CA1149384A (fr)	1983-07-05	Derives d'acide 4-nitro-2-trichloromethyl- benzenesulfenique, leur preparation et fongicides qui en renferment
US4359471A (en)	1982-11-16	2-(N-Aryl,N-1,2,3-thiadiazolylcarbonyl)-aminobutyro-lactones, their preparation, fungicidal agents containing these compounds, and their use as fungicides
US4698357A (en)	1987-10-06	2,4-dichloro-5-nitro-thiazole
EP0033114B1 (fr)	1983-08-24	Thiourées fongicides substituées, leur préparation, leur utilisation dans la lutte contre les champignons et compositions les contenant
DE3202298A1 (de)	1983-08-18	Neue 5-nitrobenzisothiazol-3-sulfide, ihre herstellung und verwendung zur bekaempfung von fungi
DE2948672A1 (de)	1981-06-25	Trialkylisilyl-benzimidazol-2-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als fungizide
EP0073973A1 (fr)	1983-03-16	Anilides d'acides thiazolyl- et isothiazolyl carboxyliques, procédé pour les préparer et leur utilisation comme fongicides
EP0092095A2 (fr)	1983-10-26	(Trihalométhyl-sulfényl)-1-méthyl-4-imidazole-carboxamide-5 et fongicides les contenant
US4562208A (en)	1985-12-31	N-Sulphenylated ureas, microbicidal agents containing these compounds and their use
DE2722035A1 (de)	1978-11-30	1,3-bis-(trihalogenmethyl-sulfenyl)- imidazolidin-2,4-dione