144090-61-9

Basic information

• Product Name: (S)-4-((S)-4-Azido-3-benzyloxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
• Synonyms: (S)-4-((S)-4-Azido-3-benzyloxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester
• CAS NO: 144090-61-9
• Molecular Weight: 404.509
• Mol File: 144090-61-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-4-((S)-4-Azido-3-benzyloxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-((S)-4-Azido-3-benzyloxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester(144090-61-9)
• EPA Substance Registry System: (S)-4-((S)-4-Azido-3-benzyloxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester(144090-61-9)

Safety Data

• Hazardous Substances Data: 144090-61-9(Hazardous Substances Data)

Upstream product

• 144090-58-4 (S)-2,2-Dimethyl-4-(2-oxiranyl-ethyl)-oxazolidine-3-carboxylic acid tert-butyl ester 
• 144090-57-3 tert-butyl (S)-4-(but-3-enyl)-2,2-dimethyloxazolidine-3-carboxylate 
• 163072-64-8 Benzoic acid (1S,4S)-4-[tert-butoxycarbonyl-(4-methoxy-benzyl)-amino]-5-hydroxy-1-hydroxymethyl-pentyl ester 
• 163072-65-9 Benzoic acid (1S,4S)-4-tert-butoxycarbonylamino-5-hydroxy-1-hydroxymethyl-pentyl ester 
• 163072-66-0 (S)-4-((S)-3,4-Dihydroxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 144090-58-4 (S)-2,2-Dimethyl-4-((S)-2-oxiranyl-ethyl)-oxazolidine-3-carboxylic acid tert-butyl ester 
• 100-39-0 benzyl bromide 
• 144090-59-5 (S)-4-((S)-4-Azido-3-hydroxy-butyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 

Downstream Products

• 121447-31-2 (2S,5R)-2,6-Bis-benzyloxycarbonylamino-5-hydroxy-hexanoic acid 
• 121447-31-2 (2S,5S)-2,6-Bis-benzyloxycarbonylamino-5-hydroxy-hexanoic acid 
• 96359-88-5 (2S,5R)-6-[(benzyloxycarbonyl)amino]-2-[(tert-butoxycarbonyl)amino]-5-hydroxyheptanoic acid 
• 96359-88-5 (2S,5S)-6-Benzyloxycarbonylamino-2-tert-butoxycarbonylamino-5-hydroxy-hexanoic acid 
• 144090-64-2 (2S,5S)-6-Azido-5-benzyloxy-2-tert-butoxycarbonylamino-hexanoic acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 75466-93-2 [(3S,6R)-6-(Benzyloxycarbonylamino-methyl)-2-oxo-tetrahydro-pyran-3-yl]-carbamic acid benzyl ester 
• 79432-05-6 L_S-threo-2-amino-6-benzyloxycarbonylamino-5-hydroxy-hexanoic acid 
• 79432-14-7 (2S,5R)-2-amino-6-[(benzyloxycarbonyl)amino]-5-hydroxyhexanoic acid 
• 86235-37-2 Dicarbobenzoxy-allohydroxylysin-δ-lacton 
• 163072-67-1 (2S,5S)-6-Azido-5-benzyloxy-2-tert-butoxycarbonylamino-hexanoic acid pentafluorophenyl ester 
• 163072-68-2 ((3S,6S)-6-Benzyloxy-1-methyl-2-oxo-azepan-3-yl)-carbamic acid tert-butyl ester 
• 144090-63-1 (2S,5S)-6-Azido-5-benzyloxy-2-tert-butoxycarbonylamino-hexanoic acid 
• 144090-65-3 ((3S,6S)-6-Benzyloxy-2-oxo-azepan-3-yl)-carbamic acid tert-butyl ester 
• 144090-62-0 ((1S,4S)-5-Azido-4-benzyloxy-1-hydroxymethyl-pentyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Stereoselective Conversion of L-Quebrachitol into a Novel Hydroxylated Caprolactam: Total Synthesis of Bengamide B

The stereoselective synthesis of the novel marine natural product, bengamide B (1), starting from L-quebrachitol (3) is described.The hydroxylated caprolactam portion (2a) in 1 was prepared from (+)-conduramine derivative (7), whose amino functionality wa