70147-48-7

Basic information

• Product Name: 2C-Hydroxymethyl-2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone
• Synonyms: 2C-Hydroxymethyl-2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone;2-C-(Hydroxymethyl)-2,3:5,6-bis-O-(1-methylethylidene)-D-mannonic acid gamma-lactone
• CAS NO: 70147-48-7
• Molecular Formula: C13H20O7
• Molecular Weight: 288.294
• Mol File: 70147-48-7.mol
• Article Data: 4

Chemical Properties

• Melting Point: 130-132 °C
• Boiling Point: 415.1±45.0 °C(Predicted)
• Appearance: /
• Density: 1.268±0.06 g/cm3(Predicted)
• PKA: 13.85±0.10(Predicted)
• CAS DataBase Reference: 2C-Hydroxymethyl-2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone(CAS DataBase Reference)
• NIST Chemistry Reference: 2C-Hydroxymethyl-2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone(70147-48-7)
• EPA Substance Registry System: 2C-Hydroxymethyl-2,3:5,6-di-O-isopropylidene-D-mannono-1,4-lactone(70147-48-7)

Safety Data

• Hazardous Substances Data: 70147-48-7(Hazardous Substances Data)

Upstream product

• 57-48-7 D-Fructose 
• 143-33-9 sodium cyanide 
• 67-64-1 acetone 
• 14131-84-1 2,3:5,6-di-O-isopropylidene-α-D-mannofuranose 
• 773837-37-9 sodium cyanide 
• 87-81-0 D-tagatose 
• 7757-38-2 2,3,5,6-di-O-isopropylidene-D-mannofuranose 

Downstream Products

• 211623-13-1 (3aS,6R,6aS)-3a-((benzyloxy)methyl)-6-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one 

Relevant articles and documents

MANNOSE DERIVATIVES FOR TREATING BACTERIAL INFECTIONS

The present invention relates to compounds useful for the treatment or prevention of bacteria infections. These compounds have formula I: The invention also provides processes for making the compounds described herein. Furthermore, the present invention p

Doubly carbon-branched pentoses: synthesis of both enantiomers of 2,4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose using only acetonide protection

An acetonide is the only protecting group used in the synthesis of both the enantiomers of 2,4-di-C-methyl arabinose and 2-deoxy-2,4-di-C-methyl arabinose via the enantiomeric 3-C-methyl-l-erythronolactone [from 2-C-methyl-d-ribono-lactone or d-ribose] and 3-C-methyl-d-erythronolactone [from d-tagatose or l-ribose]. NMR studies on unprotected C-methyl arabinoses show that methyl branching significantly affects the ratios of pyranose and furanose forms present in aqueous solution.