1439462-62-0

Basic information

• Product Name: dimethyl-{3-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-2-oxo-4-phenyl-butyl}phosphonate
• Synonyms: dimethyl-{3-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-2-oxo-4-phenyl-butyl}phosphonate
• CAS NO: 1439462-62-0
• Molecular Weight: 453.496
• Mol File: 1439462-62-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: dimethyl-{3-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-2-oxo-4-phenyl-butyl}phosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl-{3-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-2-oxo-4-phenyl-butyl}phosphonate(1439462-62-0)
• EPA Substance Registry System: dimethyl-{3-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-2-oxo-4-phenyl-butyl}phosphonate(1439462-62-0)

Safety Data

• Hazardous Substances Data: 1439462-62-0(Hazardous Substances Data)

Upstream product

• 773-64-8 2-mesitylenesulphonyl chloride 
• 5619-07-8 methyl 2-amino-3-phenylpropanoate hydrochloride 
• 1439462-50-6 methyl-2-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-3-phenyl-propionate 
• 756-79-6 dimethyl methane phosphonate 

Downstream Products

• 1439462-74-4 (4E)-2-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-1-phenyl-4-hexen-3-one 
• 1439462-80-2 (4E)-2-[N-(2,4,6-trimethylbenzenesulfonyl)amino]-7-methyl-1-phenyl-4-octen-3-one 

Relevant articles and documents

Palladium-catalyzed highly regio- and stereoselective carbon-carbon bond formation reaction of γ-substituted vinylaziridines with a silylated masked acyl cyanide reagent

Highly regio- and stereoselective carbon-carbon bond formation reaction of vinylaziridines using a masked acyl cyanide reagent possessing a tert-butyldimethylsilyl group occurred in the presence of a catalytic amount of palladium complex in excellent yield. It is considered that these excellent selectivities are the result of three simultaneous conditions, strained leaving group, small nucleophile, and ligand with small cone-angle.