94518-64-6

Basic information

• Product Name: Carbonochloridimidothioic acid, (2,6-dimethylphenyl)-, methyl ester
• CAS NO: 94518-64-6
• Molecular Formula: C10H12ClNS
• Molecular Weight: 213.731
• Mol File: 94518-64-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbonochloridimidothioic acid, (2,6-dimethylphenyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonochloridimidothioic acid, (2,6-dimethylphenyl)-, methyl ester(94518-64-6)
• EPA Substance Registry System: Carbonochloridimidothioic acid, (2,6-dimethylphenyl)-, methyl ester(94518-64-6)

Safety Data

• Hazardous Substances Data: 94518-64-6(Hazardous Substances Data)

Upstream product

• 5813-48-9 Methanesulfenyl chloride 
• 119072-54-7 2,6-dimethylphenyl isonitrile 

Downstream Products

• 118514-82-2 1-(2,6-dimethylphenyl)-4,4-diphenyl-2-(methylthio)-1,3-diazabuta-1,3-diene 
• 94518-78-2 2-({[(Z)-2,6-Dimethyl-benzylimino]-methylsulfanyl-methylimino}-methylene)-3,3-diphenyl-butyric acid methyl ester 
• 94518-68-0 2,3-Dicyano-2-{[(Z)-2,6-dimethyl-phenylimino]-methylsulfanyl-methyl}-3,3-diphenyl-propionic acid methyl ester 
• 94518-76-0 3-Cyano-2-({[(Z)-2,6-dimethyl-phenylimino]-methylsulfanyl-methylimino}-methylene)-3,3-diphenyl-propionic acid methyl ester 
• 94519-02-5 3-Cyano-2-[1-(2,6-dimethyl-phenyl)-5-[(Z)-2,6-dimethyl-phenylimino]-2-methylsulfanyl-1,5-dihydro-imidazol-(4E)-ylidene]-3,3-diphenyl-propionic acid methyl ester 
• 104157-45-1 N-(2,6-dimethylphenyl)(methylthio)formimidoyl isothiocyanate 
• 118514-98-0 1-(2,6-dimethylphenyl)-4,4-diphenyl-5-imino-2-(methylthio)-2-imidazoline 
• 118514-93-5 5-(tert-butylimino)-1-(2,6-dimethylphenyl)-4,4-diphenyl-2-(methylthio)-2-imidazoline 

Relevant articles and documents

Three-Component Cyclocondensations. Two Methods for the Efficient Preparation of 5-Aminothiazolium Salts via the Reaction of Isocyanides Either with Dimethylthioformamide and Imino Chloro Sulfides or Benyaldimines and Aryl Chlorothioformates

Treatment of imino chloro sulfides with dimethylthioformamide and isocyanides at room temperature provides selectively the 5-amino-4-(dimethylamino)-2-(methylthio) (or phenylthio)thiazolium salts.Similarly, the reactions of p-tolyl chlorothionoformate and phenyl chlorodithioformate with a mixture of benzaldimine and isocyanide afford rapidly the 5-amino-4-phenylthiazolium salts.We suggest that these reactions involve the N-(thiocarbonyl)formamidinium and benzylideniminium chlorides as transient intermediates, which are trapped by isocyanides according to a cycloaddition process.The structure of the thiazolium salts and some of their reactivities are discussed.