59055-61-7

Basic information

• Product Name: 6-Deoxy-2-O,3-O,4-O-tribenzyl-α-L-mannopyranosyl bromide
• Synonyms: 6-Deoxy-2-O,3-O,4-O-tribenzyl-α-L-mannopyranosyl bromide
• CAS NO: 59055-61-7
• Molecular Formula: C₂₇H₂₉BrO₄
• Molecular Weight: 497.42076
• Mol File: 59055-61-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-Deoxy-2-O,3-O,4-O-tribenzyl-α-L-mannopyranosyl bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Deoxy-2-O,3-O,4-O-tribenzyl-α-L-mannopyranosyl bromide(59055-61-7)
• EPA Substance Registry System: 6-Deoxy-2-O,3-O,4-O-tribenzyl-α-L-mannopyranosyl bromide(59055-61-7)

Safety Data

• Hazardous Substances Data: 59055-61-7(Hazardous Substances Data)

Usage

General Description

6-Deoxy-2-O,3-O,4-O-tribenzyl-α-L-mannopyranosyl bromide is a complex chemical compound with a molecular structure consisting of a mannose sugar molecule that has been modified with three benzyl groups and a bromine atom. 6-Deoxy-2-O,3-O,4-O-tribenzyl-α-L-mannopyranosyl bromide is commonly used in organic chemistry as a building block for the synthesis of more complex carbohydrates and glycosides. Its unique structure and reactivity make it a valuable reagent for the creation of diverse molecular structures, particularly in the field of carbohydrate chemistry. The tribenzyl-α-L-mannopyranosyl bromide has potential applications in medicinal chemistry, drug development, and the study of carbohydrate-protein interactions. Overall, this compound plays a significant role in the synthesis and manipulation of complex carbohydrates in chemical research and development.

Upstream product

• 100-44-7 benzyl chloride 
• 80161-75-7 Benzyl-2,3,4-tri-O-benzyl-β-L-rhamnopyranosid 
• 210426-02-1 2,3,4-tri-O-benzyl-L-rhamnopyranose 
• 80152-99-4 1-O-acetyl-2,3,4-tri-O-benzyl-6-deoxy-α-L-mannose 
• 128962-63-0 ethyl 2,3,4-tri-O-benzyl-1-thio-α-L-rhamanopyranoside 

Downstream Products

• 80153-01-1 Benzyl-4-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid 
• 111819-77-3 methyl 3,4,6-tri-O-benzyl-2-O-(2,3,4-tri-O-benzyl-αβ-L-rhamnopyranosyl)-β-D-glucopyranoside 
• 126330-72-1 (3aR,4R,6S,7S,7aR)-4-Methoxy-2,2,6-trimethyl-7-((2S,3R,4R,5S,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-[1,3]dioxolo[4,5-c]pyran 
• 128962-64-1 methyl 2-O-β-L-rhamnopyranosyl-β-D-galactopyranoside 
• 80153-08-8 (2R,3R,4S,5S,6S)-2,5-Bis-benzyloxy-6-methyl-4-((2S,3R,4R,5S,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-ol 
• 80153-07-7 Benzyl-4-O-benzyl-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid 
• 80153-02-2 Benzyl-4-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid 
• 88509-56-2 2-Acetamido-1,6-anhydro-4-O-benzyl-2-desoxy-3-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-β-D-galactopyranosid 
• 88509-57-3 2-Acetamido-1,6-anhydro-4-O-benzyl-2-desoxy-3-O-(2,3,4-tri-O-benzyl-α-L-rhamnopyranosyl)-β-D-galactopyranosid 
• 2374-40-5 2-Acetamido-2-desoxy-3-O-β-L-rhamnopyranosyl-D-galactopyranose 
• 88493-94-1 Benzyl O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-(1->4)-O-(2-O-allyl-3-O-benzyl-β-L-rhamnopyranosyl)-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranosid 
• 86449-22-1 Benzyl-2,3-di-O-benzyl-4-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-α-L-rhamnopyranosid 
• 86449-25-4 Benzyl-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-(1->4)-O-(2-O-allyl-3-O-benzyl-β-L-rhamnopyranosyl)-(1->4)-2,3-di-O-isopropyliden-α-L-rhamnopyranosid 
• 129031-01-2 methyl 3-O-benzyl-4,6-O-benzylidene-2-O-(2,3,4-tri-O-benzyl-β-L-rhamnopyranosyl)-β-D-galactopyranoside 

Relevant articles and documents

Synthesis of di- and tri-saccharides related to the polysaccharide from Streptococcus pneumoniae type 23 and a study of their inhibition in the precipitin reaction.

Syntheses of methyl 2-O-beta-L-rhamnopyranosyl-beta-D-galactopyranoside (9), methyl 2-O-alpha-L-rhamnopyranosyl-beta-D-galactopyranoside (13), and methyl 4-O-beta-D-glucopyranosyl-2-O-alpha-L-rhamnopyranosyl-beta-D- galactopyranoside (16) in good yields a