1,2,3,5-Tetra-O-acetyl-α-D-arabinofuranose

• Catalog No.: 634808
• CAS Number: 43225-70-3
• M. F.: C13H18O9
• M. W.: 318.27662
• Purity: ≥80%

SYNONYMS

• Title: 1,2,3,5-四-O-乙酰基-α-D-阿拉伯呋喃糖
• IUPAC name: [(2R,3R,4S,5R)-3,4,5-tris(acetyloxy)oxolan-2-yl]methyl acetate
• IUPAC Traditional name: [(2R,3R,4S,5R)-3,4,5-tris(acetyloxy)oxolan-2-yl]methyl acetate
• Synonyms: NSC 108078

DATABASE IDS

• CAS Number: 43225-70-3
• MDL Number: MFCD05865195
• PubChem SID: 24882691

PROPERTIES

• Empirical Formula (Hill Notation): C13H18O9
• Grade: technical grade
• Purity: ≥80%
• Boiling Point: 140 °C/0.01 mmHg(lit.)
• Density: 1.31 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.4500(lit.)
• GHS Signal Word: Danger
• GHS Hazard statements: H318
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P280-P305 + P351 + P338
• Risk Statements: 41
• Safety Statements: 26-39
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (English)

Packaging
5 g in glass bottle
Application
Reactant for:
• Asymmetric synthesis of hydroxyl acetylpentofuranosides via diastereoselective enzymic deacetylation through Candida antarctica B lipase (CAL B)-catalyzed alcoholysis1
• Reaction with trimethylaluminum in synthesis of 1,2-O-isopropylidene D-ribofuranose2
• Synthesis of oligosaccharides of motifs D and E of arabinogalactan present in Mycobacterium tuberculosis via coupling and glycosylation reactions3

Description (简体中文)

包装
5 g in glass bottle
Application
Reactant for:
• Asymmetric synthesis of hydroxyl acetylpentofuranosides via diastereoselective enzymic deacetylation through Candida antarctica B lipase (CAL B)-catalyzed alcoholysis1
• Reaction with trimethylaluminum in synthesis of 1,2-O-isopropylidene D-ribofuranose2
• Synthesis of oligosaccharides of motifs D and E of arabinogalactan present in Mycobacterium tuberculosis via coupling and glycosylation reactions3