185549-60-4

Basic information

• Product Name: Methyl 2,3,4-tri-O-acetyl-1-thio-α-D-xylopyranoside
• CAS NO: 185549-60-4
• Molecular Weight: 306.337
• Mol File: 185549-60-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Methyl 2,3,4-tri-O-acetyl-1-thio-α-D-xylopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl 2,3,4-tri-O-acetyl-1-thio-α-D-xylopyranoside(185549-60-4)
• EPA Substance Registry System: Methyl 2,3,4-tri-O-acetyl-1-thio-α-D-xylopyranoside(185549-60-4)

Safety Data

• Hazardous Substances Data: 185549-60-4(Hazardous Substances Data)

Upstream product

• 17314-32-8 tributyl(methylthio)stannane 
• 4049-33-6 tetra-O-acetyl-β-D-xylopyranose 

Relevant articles and documents

Synthesis of O-alpha-D-glucopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-O-alpha -D-xylopyranosyl-(1----4)-D-glucopyranose as a substrate analogue of alpha amylase.

The tetrasaccharide a-D-Glcp-(1----4)-a-D-Xylp-(1----4)-a-D-Xylp-(1----4)-D- Glcp (1) has been synthesized, as a substrate analogue of alpha amylase, by silver perchlorate-catalyzed glycosylation of benzyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-a-D-xylopyranosyl)-beta-D- glucopyranoside (30) with 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D- glucopyranosyl)-a-D-xylopyranosyl chloride or by methyl triflate-promoted condensation of 30 with methyl 2,3-di-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-a-D-glucopyranosyl)-1-thio- beta-D-xylopyranoside, followed by removal of protecting groups of the resulting tetrasaccharide derivative 40.