153923-40-1

Basic information

• Product Name: 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl bromide
• Synonyms: 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl bromide
• CAS NO: 153923-40-1
• Molecular Weight: 659.487
• Mol File: 153923-40-1.mol

Chemical Properties

• CAS DataBase Reference: 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl bromide(153923-40-1)
• EPA Substance Registry System: 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranosyl bromide(153923-40-1)

Safety Data

• Hazardous Substances Data: 153923-40-1(Hazardous Substances Data)

Upstream product

• 275358-18-4 1-O-Acetyl-2,3,4,6-tetra-O-benzoyl-α,β-galactofuranose 
• 417717-54-5 n-octyl 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranoside 
• 98-88-4 benzoyl chloride 
• 166021-57-4 n-octyl β-D-galactofuranoside 
• 2782-07-2 D-galactono-1,4-lactone 
• 5531-48-6 2,3,5,6-tetra-O-benzoyl-D-galactofuranose 
• 35556-50-4 2,3,5,6-tetra-O-benzoyl-D-galactono-1,4-lactone 
• 138811-45-7 1,2,3,5,6-penta-O-benzoyl-D-galactofuranose 
• 10257-28-0 D-Galactose 

Downstream Products

• 153809-64-4 dibenzyl 2,3,5,6-tetra-O-benzoyl-α-D-galactofuranosyl-1-phosphate 
• 417717-54-5 n-octyl 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranoside 
• 108223-94-5 2,3,5,6-tetra-O-benzoyl-β-D-galactofuranose 

Relevant articles and documents

Synthesis and biological properties of galactofuranosyl-containing fluorescent dyes

Two fluorescent galactofuranosides were synthesized and their biological activities evaluated on non-infected and Leishmania infected macrophages. Both tagged scaffolds were able to penetrate macrophages. Compared to the activity of the parent octyl galactofuranoside used as a reference, the fluorescein-conjugate showed altered biological properties while the rhodamine 6G one synergistically acted with the lipid chain to significantly increase antiparasitic activity.

Studies of UDP-galactopyranose mutase from Escherichia coli: An unusual role of reduced FAD in its catalysis

The galactofuranose moiety found in many surface constituents of microorganisms is derived from UDP-D-galactopyranose (UDP-Galp) via a unique ring contraction reaction catalyzed by UDP-Galp mutase. This enzyme, which has been isolated from several bacteri

Reactions of per-O-benzoyl-β-D-galf isothiocyanate, a chiral resolving agent

Tetra-O-benzoyl-β-D-galactofuranosyl isothiocyanate (1) was readily prepared (90% yield) from per-O-benzoyl-D-galactofuranose, via the glycosyl bromide. Reaction of 1 with alcohols, amines and amino acids afforded a variety of glycosylthiourethanes and glycosylthioureides. The isothiocyanate 1 showed to be useful as a chiral resolving agent. The resolution of recemic primary and secondary mines and aminoalcohols was readily accomplished, in analytical and preparative scale, by condensation of such compounds with 1.

A D-ribofuranosylenamine as glycosyl acceptor

Monosaccharide gycosylamines are widely know carbohydrate derivatives of interest as building blocks in the syntheses of complex glycoconjugates and neogly-coconjugates and have also been used in the prepatations of N-nucleosides, glycosyl isothiocyanates