851596-56-0

Basic information

• Product Name: [(benzyl-methoxy-carbamoyl)-methyl]-carbamic acid benzyl ester
• Synonyms: [(benzyl-methoxy-carbamoyl)-methyl]-carbamic acid benzyl ester
• CAS NO: 851596-56-0
• Molecular Weight: 328.368
• Mol File: 851596-56-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(benzyl-methoxy-carbamoyl)-methyl]-carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(benzyl-methoxy-carbamoyl)-methyl]-carbamic acid benzyl ester(851596-56-0)
• EPA Substance Registry System: [(benzyl-methoxy-carbamoyl)-methyl]-carbamic acid benzyl ester(851596-56-0)

Safety Data

• Hazardous Substances Data: 851596-56-0(Hazardous Substances Data)

Upstream product

• 20056-98-8 N-benzyl-N-methoxyamine 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 

Downstream Products

• 851596-59-3 2-(benzhydrylidene-amino)-N-benzyl-N-methoxy-3-naphthalen-1-yl-propionamide 
• 599177-29-4 (R)-2-(Benzhydrylidene-amino)-pent-4-enoic acid benzyl-methoxy-amide 
• 851596-61-7 2-(benzhydrylidene-amino)-N-benzyl-N-methoxy-butyramide 
• 599177-26-1 2-(benzhydrylidene-amino)-N-benzyl-N-methoxy-acetamide 

Relevant articles and documents

Highly enantioselective phase-transfer-catalyzed alkylation of protected α-amino acid amides toward practical asymmetric synthesis of vicinal diamines, α-amino ketones, and α-amino alcohols

Highly enantioselective alkylation of protected glycine diphenylmethyl (Dpm) amide 1 and Weinreb amide 10 has been realized under phase-transfer conditions by the successful utilization of designer chiral quaternary ammonium salts of type 4 as catalyst. P