58456-27-2

Basic information

• Product Name: (S)-3-(benzyloxycarbonyl)-4-(4-diazo-3-oxobutyl)-5-oxazolidinone
• Synonyms: (S)-3-(benzyloxycarbonyl)-4-(4-diazo-3-oxobutyl)-5-oxazolidinone
• CAS NO: 58456-27-2
• Molecular Weight: 317.301
• Mol File: 58456-27-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-3-(benzyloxycarbonyl)-4-(4-diazo-3-oxobutyl)-5-oxazolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-(benzyloxycarbonyl)-4-(4-diazo-3-oxobutyl)-5-oxazolidinone(58456-27-2)
• EPA Substance Registry System: (S)-3-(benzyloxycarbonyl)-4-(4-diazo-3-oxobutyl)-5-oxazolidinone(58456-27-2)

Safety Data

• Hazardous Substances Data: 58456-27-2(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 58456-26-1 (S)-4-<2'-(Chloroformyl)ethyl>-5-oxooxazolidin-3-carbonsaeure-benzylester 
• 56-86-0 L-glutamic acid 
• 23632-67-9 (S)-3-[3-(benzyloxycarbonyl)-5-oxooxazolidin-4-yl]propanoic acid 
• 1155-62-0 N-benzyloxycarbonyl-L-glutamic acid 

Downstream Products

• 58456-29-4 (S)-N-benzyl-2-(benzyloxycarbonylamino)-6-diazo-5-oxohexanamide 
• 58456-30-7 (S)-N-benzyl-2-(benzyloxycarbonylamino)-6-chloro-5-oxohexanamide 
• 126046-27-3 (2S)-5-oxo-2-[N-(benzyloxycarbonyl)-amino]hexanoic acid methyl ester 
• 89662-54-4 (S)-2-(benzyloxycarbonylamino)-5-oxo-hexanamide 
• 309928-96-9 (2S,5R)-6-azido-2-benzyloxycarbonylamino-5-hydroxyhexanoic acid 
• 309928-97-0 (2S,5S)-6-azido-2-benzyloxycarbonylamino-5-hydroxyhexanoic acid 
• 309928-92-5 methyl (S)-6-azido-2-benzyloxycarbonylamino-5-oxohexanoate 
• 309928-94-7 (2S,5R)-5-azidomethyl-2-benzyloxycarbonylamino-δ-valerolactone 
• 309928-95-8 (2S,5S)-5-azidomethyl-2-benzyloxycarbonylamino-δ-valerolactone 
• 309928-91-4 methyl (2S)-2-benzyloxycarbonylamino-6-bromo-5-oxohexanoate 
• 504-91-6 (5R)-5-hydroxy-L-lysine 
• 18899-29-1 (2S,5S)-5-hydroxylysine 
• 15366-19-5 methyl (S)-2-benzyloxycarbonylamino-6-diazo-5-oxohexanoate 
• 58456-28-3 (S)-N-benzyl-2-(N-hydroxymethyl)benzyloxycarbonylamino-6-diazo-5-oxohexanamide 

Relevant articles and documents

Ultrasound mediated synthesis of 2-amino-1,3-selenazoles derived from Fmoc/Boc/Z-α-amino acids

A simple and efficient one-pot synthesis of Fmoc/Boc/Z-amino acid derived 2-amino-1,3-selenazoles by the condensation of Nα-urethane protected amino acid derived bromomethyl ketones with selenourea under the influence of ultrasound has been described. Insertion of 2-amino-1,3-selenazole moiety in the side chains of Asp and Glu has also been achieved following the similar protocol. ARKAT USA, Inc.

L-α-AMINOADIPIC ACID FROM L-GLUTAMIC ACID

A convenient procedure for the preparation of L-α-aminoadipic acid from L-glutamic acid is described.