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CasNo: 604-69-3
MF: C16H22O11
Appearance: powder
Delivery Time: 15 days
Packing: 25kg/drum
Purity: 99%
Basic Information
|
Model NO. |
604-69-3 |
Appearance |
powder |
|
Color |
Colorless |
Purity |
99% |
|
Grade Standard |
Industrial Grade |
Specification |
25kg/drum |
|
Transport Package |
Drum |
Origin |
China |
Product Description
CAS No: 604-69-3
Form:powder
Product Application
β-Pentaacetyl glucose is an irreplaceable intermediate for constructing β-glycosidic bond drugs, especially in:
Nucleotide Drug Synthesis: For β-configured nucleotide analogs like tenofovir and adefovir—after deprotecting the C₁ acetyl group, it couples with phosphate or other functional groups to form β-glycosidic bonds (natural nucleotides are predominantly β-configured).
Oligosaccharide/Polysaccharide Synthesis: Mimics natural polysaccharide β-glycosidic bonds (e.g., cellulose, starch) to synthesize functional oligosaccharides (e.g., heparin, chondroitin sulfate) for pharmaceuticals (intermediates or targeted drug carriers).
Antibiotic Synthesis: Introduces β-glycosidic structures in macrolide antibiotics (e.g., erythromycin, vancomycin) via β-pentaacetyl glucose.
β-Glycosylation Template: Acts as a β-configured glycosyl donor, undergoing β-selective glycosylation with acceptors (e.g., alcohols, amines, thiols) under Lewis acid catalysis (e.g., BF₃·Et₂O, TMSOTf) to study glycosidic bond formation mechanisms and stereoselectivity control.
Configurational Analysis Standard: Used as a reference for β-D-glucose derivatives in HPLC, NMR, and other analytical methods to distinguish α/β isomers.
Biodegradable Materials: Polymerizes via β-glycosidic bonds to produce β-glucan derivatives for drug delivery carriers, tissue engineering scaffolds, etc.
Functional Coatings: Leverages the steric hindrance of β-configuration to prepare surfaces with unique wettability or biocompatibility.
Packaging
25kg/drum
Storage
Store in a cool, dry, dark place (temperature ≤25°C, relative humidity ≤60%).