54837-18-2

Basic information

• Product Name: Butanoic acid, 2-[(phenylmethoxy)amino]-
• CAS NO: 54837-18-2
• Molecular Formula: C11H15NO3
• Molecular Weight: 209.245
• Mol File: 54837-18-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Butanoic acid, 2-[(phenylmethoxy)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanoic acid, 2-[(phenylmethoxy)amino]-(54837-18-2)
• EPA Substance Registry System: Butanoic acid, 2-[(phenylmethoxy)amino]-(54837-18-2)

Safety Data

• Hazardous Substances Data: 54837-18-2(Hazardous Substances Data)

Upstream product

• 80-58-0 2-Bromobutyric acid 
• 622-33-3 N-benzyloxyamine 
• 97-94-9 triethyl borane 
• 1556-18-9 cyclopentyl iodide 
• 77845-97-7 2-[(phenylmethoxy)imino]-acetic acid 
• 2687-43-6 O-benzylhydoxylamine hydrochloride 
• 298-12-4 Glyoxilic acid 
• 557-20-0 diethylzinc 

Downstream Products

• 86613-96-9 2-(Benzyloxy-formyl-amino)-butyric acid methyl ester 
• 73376-07-5 N-benzyloxy-DL-α-aminobutyric acid NCA 
• 112240-14-9 N-Benzyloxy-DL-α-aminobuttersaeure-benzylester 
• 95205-00-8 methyl 2-(benzyloxyamino)butanoate 

Relevant articles and documents

Enantioselective radical addition reactions to the C=N bond utilizing chiral quaternary ammonium salts of hypophosphorous acid in aqueous media

An enantioselective addition of alkyl radicals to glyoxylate oxime ether mediated by Cinchona alkaloid derived chiral ammonium salts of hypophosphorous acid, QP and QDP, has been developed. The Royal Society of Chemistry.

Stereocontrol in solid-phase radical reactions: Radical addition to oxime ether anchored to polymer support

(Matrix presented) A high degree of stereocontrol in solid-phase radical reactions was achieved by using triethylborane and diethylzinc as a radical initiator at low reaction temperature. Alkyl radical addition to Oppolzer's camphorsultam derivatives of o

Novel synthesis of α-amino acid derivatives through triethylborane- induced solid-phase radical reactions

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