313657-36-2

Basic information

• Product Name: Carbamic acid, (2-oxo-2-phenylethyl)(phenylmethyl)-, 1,1-dimethylethyl ester
• CAS NO: 313657-36-2
• Molecular Formula: C20H23NO3
• Molecular Weight: 325.408
• Mol File: 313657-36-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (2-oxo-2-phenylethyl)(phenylmethyl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (2-oxo-2-phenylethyl)(phenylmethyl)-, 1,1-dimethylethyl ester(313657-36-2)
• EPA Substance Registry System: Carbamic acid, (2-oxo-2-phenylethyl)(phenylmethyl)-, 1,1-dimethylethyl ester(313657-36-2)

Safety Data

• Hazardous Substances Data: 313657-36-2(Hazardous Substances Data)

Upstream product

• 70-11-1 α-bromoacetophenone 
• 98-86-2 acetophenone 
• 209528-77-8 N-methoxy-N-methyl-N'-benzyl-N'-tert-butyloxycarbonylglycinamide 
• 100-58-3 phenylmagnesium bromide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 50606-93-4 α-(N-Benzylamino)acetophenone 
• 100-46-9 benzylamine 

Downstream Products

• 1345985-92-3 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 4-nitrobenzenesulfonate 
• 1345985-93-4 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 4-cyanobenzenesulfonate 
• 1345985-94-5 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl naphthalene-1-sulfonate 
• 1345985-95-6 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 2-(trifluoromethyl)benzenesulfonate 
• 1345985-96-7 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl naphthalene-2-sulfonate 
• 1345985-97-8 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 4-methylbenzenesulfonate 
• 1345985-98-9 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 2,4-dinitrobenzenesulfonate 
• 1345985-87-6 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 2,3-dichlorobenzenesulfonate 
• 1345985-88-7 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 3-nitrobenzenesulfonate 
• 1345985-89-8 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 2,6-dichlorobenzenesulfonate 
• 1345985-90-1 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 4-fluorobenzenesulfonate 
• 1345985-91-2 2-(benzyl(tert-butoxycarbonyl)amino)-1-phenylethyl 3,5-dimethylbenzenesulfonate 
• 51096-49-2 (S)-(+)-2-(N-Benzylamino)-1-phenylethanol 
• 27159-38-2 (R)-(-)-N-Benzyl-2-phenylaziridine 

Relevant articles and documents

Synthesis and 2D QSAR of O-sulphonated β-aminols derivatives as novel antifungal and antibacterial agents

Synthesis of a series of b-aminol derivatives using regioselective opening reaction catalyzed by SiO2 (60-120 mesh) and O-sulphonation in THF-KOH system, comprising tert-butoxycarbonyl at secondary nitrogen and evaluate for various stains of bacteria and fungi. SAR study of synthesized compound using backward regression analysis.

Enantioselective synthesis of β-hydroxy amines and aziridines using asymmetric transfer hydrogenation of α-amino ketones

Enantioselective transfer hydrogenation of α-amino ketones is an effective method for the asymmetric synthesis of β-hydroxy amines and aziridines.