289901-76-4

Basic information

• Product Name: ethyl 2,3,4-tri-O-benzyl-6-deoxy-1-thio-β-D-glucopyranoside
• Synonyms: ethyl 2,3,4-tri-O-benzyl-6-deoxy-1-thio-β-D-glucopyranoside
• CAS NO: 289901-76-4
• Molecular Weight: 478.653
• Mol File: 289901-76-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl 2,3,4-tri-O-benzyl-6-deoxy-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2,3,4-tri-O-benzyl-6-deoxy-1-thio-β-D-glucopyranoside(289901-76-4)
• EPA Substance Registry System: ethyl 2,3,4-tri-O-benzyl-6-deoxy-1-thio-β-D-glucopyranoside(289901-76-4)

Safety Data

• Hazardous Substances Data: 289901-76-4(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 488-79-9 6-deoxy-D-glucose 
• 289901-74-2 1,2,3,4-tetra-O-benzoyl-6-deoxy-D-glucopyranose 
• 6087-46-3 methyl 2,3,4-tri-O-acetyl-6-chloro-6-deoxy-α-D-glucopyranoside 
• 19940-17-1 methyl 2,3,4-tri-O-acetyl-6-deoxy-α-D-glucopyranoside 
• 289901-75-3 ethyl 2,3,4-tri-O-benzoyl-6-deoxy-1-thio-β-D-glucopyranoside 
• 4144-87-0 methyl 6-chloro-6-deoxy-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 

Downstream Products

• 24809-76-5 6-Desoxy-α-D-glucopyranosyl-phosphat 
• 19083-14-8 uridine 5'-(6-deoxy-α-D-glucopyranosyl diphosphate) 
• 24988-24-7 thymidine 5'-(6-deoxy-α-D-glucopyranosyl diphosphate) 
• 120449-27-6 dibenzyl-(2,3,4-tri-O-benzyl-6-deoxy-α-D-glucopyranosyl) phosphate 

Relevant articles and documents

Active-site engineering of nucleotidylyltransferases and general enzymatic methods for the synthesis of natural and "unnatural" UDP- and TDP-nucleotide sugars

The present invention provides mutant nucleotidylyl-transferases, such as Ep, having altered substrate specificity; methods for their production; and methods of producing nucleotide sugars, which utilize these nucleotidylyl-transferases. The present invention also provides methods of synthesizing desired nucleotide sugars using natural and/or modified Ep or other nucleotidyltransferases; and nucleotide sugars sythesized by the present methods. The present invention further provides new glycosyl phosphates, and methods for making them.