1146393-55-6

Basic information

• Product Name: (1S,2S,3R,5R)-3-(benzyloxy)-2-hydroxy-5-(hydroxymethyl)cyclopentyl pivalate
• Synonyms: (1S,2S,3R,5R)-3-(benzyloxy)-2-hydroxy-5-(hydroxymethyl)cyclopentyl pivalate
• CAS NO: 1146393-55-6
• Molecular Weight: 322.401
• Mol File: 1146393-55-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,3R,5R)-3-(benzyloxy)-2-hydroxy-5-(hydroxymethyl)cyclopentyl pivalate(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,3R,5R)-3-(benzyloxy)-2-hydroxy-5-(hydroxymethyl)cyclopentyl pivalate(1146393-55-6)
• EPA Substance Registry System: (1S,2S,3R,5R)-3-(benzyloxy)-2-hydroxy-5-(hydroxymethyl)cyclopentyl pivalate(1146393-55-6)

Safety Data

• Hazardous Substances Data: 1146393-55-6(Hazardous Substances Data)

Upstream product

• 1146393-45-4 ((1R,2R,4R,5S)-4-(benzyloxy)-6-oxabicyclo[3.1.0]hexan-2-yl)methyl pivalate 

Relevant articles and documents

Studies toward the total synthesis of carba analogue of motif C of M. TB cell wall AG complex

Herein we describe the synthesis of the carba analogue of motif C of arabinogalactan complex present in M. tuberculosis cell wall. Pd(0) catalyzed allylic alkylation and Fraser-Reid's glycosidation are the two key reactions that were employed for the synthesis of central glycosyl accepter unit and the glycosylation respectively.