25983-70-4

Basic information

• Product Name: benzyl N-[2-(benzyloxyamino)-2-oxoethyl]carbamate
• Synonyms: benzyl N-[2-(benzyloxyamino)-2-oxoethyl]carbamate
• CAS NO: 25983-70-4
• Molecular Weight: 314.341
• Mol File: 25983-70-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: benzyl N-[2-(benzyloxyamino)-2-oxoethyl]carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl N-[2-(benzyloxyamino)-2-oxoethyl]carbamate(25983-70-4)
• EPA Substance Registry System: benzyl N-[2-(benzyloxyamino)-2-oxoethyl]carbamate(25983-70-4)

Safety Data

• Hazardous Substances Data: 25983-70-4(Hazardous Substances Data)

Upstream product

• 1212-53-9 methyl N-benzyloxycarbonylglycinate 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 

Relevant articles and documents

Catalyst-Controlled Regiodivergent Synthesis of α/β-Dipeptide Derivatives via N-Allylic Alkylation of O-Alkyl Hydroxamates with MBH Carbonates

A controllable and regiodivergent N-allylation reaction involving readily available O-alkyl hydroxamates derived from natural α-amino acids has been developed, allowing regiospecific access to α/β-dipeptides containing α-unsaturated β-amino acids moieties in moderate to good yields. The regioselectivity could be conveniently switched by alternation of the catalysts and solvents.

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE

The invention relates to a compound of Formula (I), or pharmaceutically acceptable enantiomers, or salts thereof. The present invention also relates to the use of compounds of Formula (I) as selective inhibitors of indoleamine 2,3-dioxygenase. The inventi

A Convenient Procedure for the Preparation of Amino Acid Hydroxamates from Esters

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