133760-23-3

Basic information

• Product Name: 2-benzyloxycarbonylamino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylitol
• Synonyms: 2-benzyloxycarbonylamino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylitol
• CAS NO: 133760-23-3
• Molecular Weight: 563.766
• Mol File: 133760-23-3.mol

Chemical Properties

• CAS DataBase Reference: 2-benzyloxycarbonylamino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylitol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyloxycarbonylamino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylitol(133760-23-3)
• EPA Substance Registry System: 2-benzyloxycarbonylamino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylitol(133760-23-3)

Safety Data

• Hazardous Substances Data: 133760-23-3(Hazardous Substances Data)

Upstream product

• 126448-11-1 4-benzyloxycarbonylamino-1-O-tert-butyldiphenylsilyl-4,5-dideoxy-2,3-O-(1-methylethylidene)-5-phenylsulfinyl-D-xylitol 
• 126448-10-0 4-benzyloxycarbonylamino-1-O-tert-butyldiphenylsilyl-2,3-O-(1-methylethylidene)-4,5-dideoxy-5-phenylthio-D-xylitol 
• 126448-09-7 4-benzyloxycarbonylamino-4,5-dideoxy-2,3-O-(1-methylethylidene)-5-phenylthio-D-xylose diethyl dithioacetal 
• 126448-16-6 [(S)-1-((4S,5R)-5-Formyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenylsulfanyl-ethyl]-carbamic acid benzyl ester 
• 126448-08-6 4,5-(benzyloxycarbonyl)imino-4,5-dideoxy-2,3-O-(1-methylethylidene)-D-xylose diethyl dithioacetal 
• 126448-07-5 (S)-2-Azido-1-[(4S,5R)-5-(bis-ethylsulfanyl-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethanol 
• 126448-15-5 4,5-dideoxy-4,5-imino-2,3-O-(1-methylethylidene)-D-xylose diethyl dithioacetal 
• 53872-72-3 2,3-O-isopropylidene-L-arabinose diethyl mercaptal 
• 126448-19-9 2-benzyloxycarbonylamino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylose O-acetyl S-phenyl monothioacetal 
• 126448-11-1 {2-Benzenesulfinyl-1-[(S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-ethyl}-carbamic acid benzyl ester 
• 126448-10-0 {1-[(S)-5-(tert-Butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-phenylsulfanyl-ethyl}-carbamic acid benzyl ester 
• 126448-09-7 {1-[(R)-5-(Bis-ethylsulfanyl-methyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-2-phenylsulfanyl-ethyl}-carbamic acid benzyl ester 
• 126448-16-6 [1-((R)-5-Formyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenylsulfanyl-ethyl]-carbamic acid benzyl ester 
• 126448-17-7 [1-((S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenylsulfanyl-ethyl]-carbamic acid benzyl ester 

Downstream Products

• 126448-13-3 2-amino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylonic acid 
• 126448-12-2 2-benzyloxycarbonylamino-5-O-tert-butyldiphenylsilyl-2-deoxy-3,4-O-(1-methylethylidene)-L-xylonic acid 
• 126448-12-2 Benzyloxycarbonylamino-[(S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-acetic acid 
• 126448-13-3 Amino-[(S)-5-(tert-butyl-diphenyl-silanyloxymethyl)-2,2-dimethyl-[1,3]dioxolan-4-yl]-acetic acid 

Relevant articles and documents

Enantiospecific synthesis of polyoxamic acid from L-arabinose

An enantiospecific synthesis of polyoxamic acid, 2-amino-2-deoxy-L-xylonic acid, by phenylthiolate opening of a five-carbon chiral hydroxylated aziridine easily derived from L-arabinose, is reported. The formation of the carboxyl group resulted from a Pum

AN ENANTIOSPECIFIC SYNTHESIS OF POLYOXAMIC ACID FROM L-ARABINOSE

Polyoxamic acid, 2-amino-2-deoxy-L-xylonic acid, is synthetized by thiopenoxide opening of a five-carbon chiral hydroxylated aziridine easily derived from L-arabinose.The formation of the carboxy group resulted from a Pummerer reaction.