1010833-16-5

Basic information

• Product Name: (5Z)-2-amino-[5-(2,4-dichlorobenzylidene)]-5,6-dihydro-1,3-thiazin-4-one
• Synonyms: (5Z)-2-amino-[5-(2,4-dichlorobenzylidene)]-5,6-dihydro-1,3-thiazin-4-one
• CAS NO: 1010833-16-5
• Molecular Weight: 287.169
• Mol File: 1010833-16-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (5Z)-2-amino-[5-(2,4-dichlorobenzylidene)]-5,6-dihydro-1,3-thiazin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5Z)-2-amino-[5-(2,4-dichlorobenzylidene)]-5,6-dihydro-1,3-thiazin-4-one(1010833-16-5)
• EPA Substance Registry System: (5Z)-2-amino-[5-(2,4-dichlorobenzylidene)]-5,6-dihydro-1,3-thiazin-4-one(1010833-16-5)

Safety Data

• Hazardous Substances Data: 1010833-16-5(Hazardous Substances Data)

Upstream product

• 17356-08-0 thiourea 
• 364633-47-6 methyl 3-(2,4-dichlorophenyl)-3-hydroxy-2-methylenepropanoate 
• 874-42-0 2,4-dichlorobenzaldeyhde 

Relevant articles and documents

Synthesis of 1,3-thiazine-2,4-diones with potential anticancer activity

2-Amino-1,3-thiazin-4-ones were subjected to acetylation followed by mild acid hydrolysis to give compounds containing the 1,3-thiazine-2,4-dione core. The potential of these S,N-containing heterocycles as antitumor agents against human cancer cell lines,

Synthesis of allylic thiocyanates and novel 1,3-thiazin-4-ones from 2-(bromomethyl)alkenoates and S-nucleophiles in aqueous medium

Allylic thiocyanates and novel heterocycles containing the 1,3-thiazin-4-one core are easily obtained in high yields and mild conditions by nucleophilic displacement of 2-(bromomethyl)alkenoates (derived from Morita-Baylis-Hillman adducts) with sulphur-ce