1607015-04-2

Basic information

• Product Name: 1-[2-(2,4-dichlorophenylimino)-3-di(dimethylamino)methyl-4-methyl-2,3-dihydro-1,3-thiazol-5-yl]-1-ethanone chloride
• CAS NO: 1607015-04-2
• Molecular Weight: 435.805
• Mol File: 1607015-04-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-[2-(2,4-dichlorophenylimino)-3-di(dimethylamino)methyl-4-methyl-2,3-dihydro-1,3-thiazol-5-yl]-1-ethanone chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-(2,4-dichlorophenylimino)-3-di(dimethylamino)methyl-4-methyl-2,3-dihydro-1,3-thiazol-5-yl]-1-ethanone chloride(1607015-04-2)
• EPA Substance Registry System: 1-[2-(2,4-dichlorophenylimino)-3-di(dimethylamino)methyl-4-methyl-2,3-dihydro-1,3-thiazol-5-yl]-1-ethanone chloride(1607015-04-2)

Safety Data

• Hazardous Substances Data: 1607015-04-2(Hazardous Substances Data)

Upstream product

• 1694-29-7 3-chloropentane-2,4-dione 
• 6590-96-1 2, 4-dichlorophenyl isothiocyanate 
• 80-70-6 N,N,N',N'-tetramethylguanidine 

Relevant articles and documents

A synthesis of functionalized 2-imino-1,3-thiazoles from tetramethylguanidine, isothiocyanates, and 2-chloro-1,3-dicarbonyl compounds

The Hantzsch method for thiazole synthesis is modified via the reaction of 2-chloro-1,3-dicarbonyl compounds with 2-(amidosulfanylenemethyl)-1,1,3,3- tetramethylguanidines (prepared in situ from tetramethylguanidine and isothiocyanates), to afford functionalized 2-imino-1,3-thiazoles in good yields. Graphical Abstract: [Figure not available: see fulltext.]