1309440-27-4

Basic information

• Product Name: benzyl 1-(methoxycarbonyl)-2-(4-methoxyphenylamino)-2-(4-nitrophenyl)-1-phenylethylcarbamate
• Synonyms: benzyl 1-(methoxycarbonyl)-2-(4-methoxyphenylamino)-2-(4-nitrophenyl)-1-phenylethylcarbamate
• CAS NO: 1309440-27-4
• Molecular Weight: 555.587
• Mol File: 1309440-27-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl 1-(methoxycarbonyl)-2-(4-methoxyphenylamino)-2-(4-nitrophenyl)-1-phenylethylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 1-(methoxycarbonyl)-2-(4-methoxyphenylamino)-2-(4-nitrophenyl)-1-phenylethylcarbamate(1309440-27-4)
• EPA Substance Registry System: benzyl 1-(methoxycarbonyl)-2-(4-methoxyphenylamino)-2-(4-nitrophenyl)-1-phenylethylcarbamate(1309440-27-4)

Safety Data

• Hazardous Substances Data: 1309440-27-4(Hazardous Substances Data)

Upstream product

• 5455-87-8 4-methoxy-N-(4-nitrobenzylidene)aniline 
• 621-84-1 O-benzyl carbamate 
• 22979-35-7 Methyl phenyldiazoacetate 

Relevant articles and documents

Diastereoselectively switchable enantioselective trapping of carbamate ammonium ylides with imines

The diastereoselectively switchable enantioselective trapping of protic carbamate ammonium ylides with imines is reported. The intriguing Rh 2(OAc)4 and chiral Bronsted acid cocatalyzed three-component Mannich-type reaction of a diazo compound, a carbamate, and an imine provides rapid and efficient access to both syn- and anti-α- substituted α,β-diamino acid derivatives with a high level control of chemo-, diastereo-, and enantioselectivity.