Acetobromo-α-D-glucose

• Catalog No.: 00530
• CAS Number: 572-09-8
• M. F.: C14H19BrO9
• M. W.: 411.19926
• Purity: ≥95.0% (AT)

SYNONYMS

• IUPAC name: [(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-bromooxan-2-yl]methyl acetate
• IUPAC Traditional name: [(2R,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-bromooxan-2-yl]methyl acetate
• Synonyms: 1-Bromo-α-D-glucose tetraacetate; 2,3,4,6-Tetra-O-acetyl-α-D-glucopyranosyl bromide

DATABASE IDS

• MDL Number: MFCD00063254
• PubChem SID: 24845061
• Beilstein Number: 96669
• CAS Number: 572-09-8

PROPERTIES

• Contains: ~1% CaCO3 as stabilizer
• Empirical Formula (Hill Notation): C14H19BrO9
• Grade: purum
• Purity: ≥95.0% (AT)
• Shipped in: dry ice
• Melting Point: 86-89 °C
• Optical Rotation: [α]20/D +195±10°, c = 3% in chloroform
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• Storage Temperature: -20°C
• German water hazard class: nwg

DETAILS

Description (English)

Other Notes
Glucose derivative used for the β-glucosylation of alcohols (Königs-Knorr synthesis) in the presence of an activator, e.g. metal salts 1,2,3; Radical substitution at C-14
Application
Acetobromo-α-D-glucose is used as a possible poly (ethylene terephthalate) (PET) surface modification reagent to increase its blood compatibility.

Description (简体中文)

Other Notes
Glucose derivative used for the β-glucosylation of alcohols (Königs-Knorr synthesis) in the presence of an activator, e.g. metal salts 1,2,3; Radical substitution at C-14
Application
Acetobromo-α-D-glucose is used as a possible poly (ethylene terephthalate) (PET) surface modification reagent to increase its blood compatibility.