7465-44-3

Basic information

• Product Name: methyl 6-bromo-6-deoxyhexopyranoside
• CAS NO: 7465-44-3
• Molecular Formula: C₇H₁₃BrO₅
• Molecular Weight: 257.0791
• Mol File: 7465-44-3.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 387.6°C at 760 mmHg
• Flash Point: 188.2°C
• Density: 1.73g/cm³
• Vapor Pressure: 1.32E-07mmHg at 25°C
• Refractive Index: 1.564
• CAS DataBase Reference: methyl 6-bromo-6-deoxyhexopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 6-bromo-6-deoxyhexopyranoside(7465-44-3)
• EPA Substance Registry System: methyl 6-bromo-6-deoxyhexopyranoside(7465-44-3)

Safety Data

• Hazardous Substances Data: 7465-44-3(Hazardous Substances Data)

Upstream product

• 10368-81-7 methyl 4-O-benzoyl-6-bromo-6-deoxy-α-D-glucopyranoside 
• 97-30-3 methyl-alpha-D-glucopyranoside 
• 7404-32-2 methyl 2,3,4-tri-O-acetyl-6-bromo-6-deoxy-α-D-glucopyranoside 

Downstream Products

• 14169-22-3 methyl 2,3,4-tri-O-benzoyl-6-bromo-6-deoxy-α-D-glucopyranoside 
• 135216-49-8 methyl 2,3-di-O-benzoyl-6-bromo-6-deoxy-α-D-glucopyranoside 
• 7404-32-2 methyl 2,3,4-tri-O-acetyl-6-bromo-6-deoxy-α-D-glucopyranoside 
• 73111-14-5 3,4,5-tris(benzyloxy)-2-(bromomethyl)-6-methoxytetrahydro-2H-pyran 
• 130471-81-7 (2S,3S,4R)-1-Benzylamino-hex-5-ene-2,3,4-triol 
• 5155-43-1 methyl 6-deoxy-α-D-glucopyranoside 
• 1373434-24-2 benzyl (2-methyl-4-((((2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-yl)methyl)sulfonyl)butan-2-yl)carbamate 
• 5155-47-5 methyl 6-amino-6-deoxy-α-D-glucopyranoside 
• 23701-87-3 methyl 6-azido-6-deoxy-α-D-glucopyranoside 
• 51236-53-4 methyl 2,3,4-tri-O-benzoyl-6-deoxy-α-D-glucopyranoside 
• 51236-52-3 methyl 2,3-di-O-benzoyl-6-deoxy-α-D-glucopyranoside 
• 51236-51-2 methyl 2,4-di-O-benzoyl-6-deoxy-α-D-glucopyranoside 
• 6893-93-2 methyl 2,3-di-O-benzoyl-6-deoxy-4-O-(p-tolylsulfonyl)-α-D-glucopyranoside 

Relevant articles and documents

A simple synthesis of 6-deoxy-D-(6-2H)glucopyranose

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A novel protocol for the regioselective bromination of primary alcohols in unprotected carbohydrates or glycosides

The regioselective and efficient bromination of primary hydroxyl groups in unprotected carbohydrates or glycosides is successfully achieved by using (chloro-phenylthio-methylene)dimethylammoniumchloride (CPMA) in the presence of tetrabutylammonium bromide

Novel drug delivery compositions

The present invention provides for a novel molecules useful for delivery of compounds to a mammal, more particularly for the intracellular delivery of nucleotides, nucleotide analogues or compounds with a heterocyclic base. Also provided for are novel therapeutic complexes comprising novel molecules complexed with nucleotide analogues or heterogeneous or homogenous oligomers comprised of nucleotide analogues.