222973-58-2

Basic information

• Product Name: methyl 2,3-di-O-benzoyl-β-L-arabinopyranozide
• Synonyms: methyl 2,3-di-O-benzoyl-β-L-arabinopyranozide
• CAS NO: 222973-58-2
• Molecular Weight: 372.375
• Mol File: 222973-58-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2,3-di-O-benzoyl-β-L-arabinopyranozide(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,3-di-O-benzoyl-β-L-arabinopyranozide(222973-58-2)
• EPA Substance Registry System: methyl 2,3-di-O-benzoyl-β-L-arabinopyranozide(222973-58-2)

Safety Data

• Hazardous Substances Data: 222973-58-2(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 222973-62-8 methyl 2-O-benzoyl-3,4-O-isopropylidene-α-L-arabinopyranoside 
• 38088-60-7 methyl 3,4-O-isopropylidene-β-L-arabinopyranoside 

Downstream Products

• 222973-63-9 methyl 2,3-di-O-benzoyl-4-deoxy-4-<(1R,4R,5S,6R)-4,5,6-tribenzyloxycyclohex-2-en-1-yl>thio-β-D-xylopyranoside 
• 222973-59-3 methyl 2,3-di-O-benzoyl-4-deoxy-4-<(1R,4R,5S,6S)-4,5,6-tribenzyloxycyclohex-2-en-1-yl>amino-β-D-xylopyranoside 
• 80245-11-0 methyl 2,3-di-O-benzoyl-α-D-xylopyranoside 
• 18390-72-2 methyl 4-azido-4-deoxy-β-L-arabinopyranoside 
• 52019-89-3 (2S,3S,4S)-2-(hydroxymethyl)pyrrolidine-3,4-diol 
• 83158-23-0 methyl 2,3-di-O-benzoyl-4-O-p-toluenesulfonyl-α-D-xylopyranoside 
• 13143-95-8 methyl 4-azido-2,3-di-O-benzoyl-4-deoxy-β-L-arabinopyranoside 
• 101242-41-5 methyl 2,3-di-O-benzoyl-4-O-trifluoromethylsulfonyl-α-L-arabinopyranoside 
• 18930-05-7 methyl 2,3-di-O-benzoyl-4-bromo-4-deoxy-D-xylopyranoside 

Relevant articles and documents

A synthesis of conduramine B and a 'condurithiol', useful molecules for studying the inhibition of β-xylosidases

Conduramine B and a 'condurithiol', namely (1S,2S,3R,6R)-6-aminocyclohex-4-ene-1,2,3-triol and 1R,2S,3R,6R)-6-sulfanylcyclohex-4-ene-1,2,3-triol, have been prepared by the thermal rearrangement of an acetimidate and a dithiocarbonate, respectively. Both the amine and the thiol are putative inhibitors of β-xylosidases and, in order to mimic the natural substrate more closely, an N- and an S-pseudo-disaccharide have been prepared.