152723-53-0

Basic information

• Product Name: 3-(3,5-dichlorophenyl)-5-methyl-5-vinyloxazolidine-2,4-dione
• CAS NO: 152723-53-0
• Molecular Weight: 286.114
• Mol File: 152723-53-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 3-(3,5-dichlorophenyl)-5-methyl-5-vinyloxazolidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,5-dichlorophenyl)-5-methyl-5-vinyloxazolidine-2,4-dione(152723-53-0)
• EPA Substance Registry System: 3-(3,5-dichlorophenyl)-5-methyl-5-vinyloxazolidine-2,4-dione(152723-53-0)

Safety Data

• Hazardous Substances Data: 152723-53-0(Hazardous Substances Data)

Upstream product

• 34893-92-0 3,4-dichlorophenyl isocyanate 
• 72531-53-4 isobutyl 2-hydroxy-2-vinylpropionate 
• 25216-51-7 3,5-dichlorophenyl-carbamic acid isobutyl ester 
• 13142-57-9 1-(3,5-Dichlorophenyl)urea 

Downstream Products

• 83792-61-4 N-(3,5-Dichlorophenyl)-2-hydroxy-2-methylbut-3-enanilide 
• 626-43-7 3,5-Dichloroaniline 
• 25217-43-0 methyl (3,5-dichlorophenyl)carbamate 
• 83015-12-7 methyl N-(3,5-dimethoxyphenyl)carbamate 
• 34893-92-0 3,4-dichlorophenyl isocyanate 
• 24261-46-9 3-(3,5-Dichlorophenyl)-5-methyl-5-methyl-oxazolidine-2,4-dione 
• 2150-88-1 methyl-N-(3-chlorophenyl)carbamate 
• 51422-77-6 (3-methoxyphenyl)carbamic acid methyl ester 
• 1016-70-2 3-(3-chlorophenyl)-5-methyloxazolidine-2,4-dione 
• 50471-45-9 5-(1-bromo-vinyl)-3-(3,5-dichloro-phenyl)-5-methyl-oxazolidine-2,4-dione 
• 119209-27-7 2-[[(3,5-dichlorophenyl)-carbamoyl]oxy]-2-methyl-3-butenoic acid 

Relevant articles and documents

Pyrimidine derivatives, process and intermediate products for their preparation and pesticides or fungicides containing these derivatives

Pyrimidine compounds I wherein X is C(CO2CH3)═NOCH3, C(CONHCH3)═NOCH3, C(CO2CH3)═CHOCH3, C(CO2CH3)═CHCH3or N(CO2CH3)—OCH3; R1, R2are hydrogen, alkyl, haloalkyl or alkoxy; A is R3is hydrogen, alkyl, haloalkyl, phenoxyalkyl, cycloalkyl, cyano, alkoxy, hydroxyl or halogen; R4is hydrogen, optionally substituted alkyl, alkenyl, alkynyl, haloalkenyl, haloalkynyl, cycloalkyl or alkoxy; Y is hydrogen, hydroxyl, halogen, optionally substituted aryl, hetaryl, cycloalkyl, cycloalkenyl, heterocyclyl, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, aryloxy, arylthio, hetaryloxy, hetarylthio, cycloalkyloxy or alkylthio, or their salt, their synthesis and intermediates therefore, and their activity against fungi or animal pests.

Use of aminoisothiazoles as microbicides

PCT No. PCT/EP97/06854 Sec. 371 Date Jun. 16, 1999 Sec. 102(e) Date Jun. 16, 1999 PCT Filed Dec. 9, 1997 PCT Pub. No. WO98/27816 PCT Pub. Date Jul. 2, 1998Aminoisothiazoles of the formula I, where R is hydrogen or C1-C4 alkyl and X is halogen, NO2, CN or SCN, and metal complexes and acid addition salts thereof are used as microbicides for protecting industrial materials from being attacked and destroyed by microorganisms.

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