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2,3,4,6-Tetra-O-benzyl-D-glucopyranose CAS-no-4132-28-9

CAS NO.:4132-28-9

White crystalline powder                   MF: C34H36O6                    MW: 540.65                      Capacity: from hundreds of KGs to Tonnage
Product Categories: Halogenated Heterocycles ,Pyrazoles;Biochemistry;Glucose;O-Substituted Sugars;Sugars;aldehydes;Carbohydrates & Derivatives;Carbohydrate Synthesis;Monosaccharides;Specialty Synthesis;Carbohydrates;Carbohydrates A to;Carbohydrates P-ZBiochemicals and Reagents;Monosaccharide

2,3,4,6-Tetra-O-benzyl-D-glucopyranose is an important D-glucopyranose derivative, which is often used as a pharmaceutical intermediate in the synthesis of derivatives for the treatment of Alzheimer’s disease, diabetes, and cancer.

Melting point  145-149 °C(lit.)
Boiling point  672.4±55.0 °C(Predicted)
density  1.22±0.1 g/cm3(Predicted)
storage temp.  Sealed in dry,Store in freezer, under -20°C
solubility  Soluble in chloroform
pka 11.87±0.70(Predicted)
form  Solid
color  White to Off-White
Optical Rotation [α]20/D +49±2°, c = 2% in dioxane
Purity 99%
                 Product manager                 Joy Wu;        Email: Joy@coreychem.com

2,3,4,6-Tetra-O-benzyl-D-glucopyranose (cas# 4132-28-9) is a compound useful in organic synthesis. For example, it enables the preparation of α-glucopyranosyl chloride as well as 1-C-α-D-glucopyranosyl derivatives; it can also be used in the preparation of important D-glucopyranosyl derivatives for glucosylation and other reactions.

2,3,4,6-Tetra-O-benzyl-D-glucopyranose is an important D-glucopyranose derivative, which is often used as a pharmaceutical intermediate in the synthesis of derivatives for the treatment of Alzheimer’s disease, diabetes, and cancer. After activation with trifluoroacetic anhydride, 2,3,4,6-Tetra-O-benzyl-D-glucopyranose reacts with various silyl enol ethers or allyl silanes in the presence of Lewis acids to generate α-configured C-D-glucopyranosyl derivatives, and reacts with activated aromatic nucleophiles to generate the corresponding β-anomers[2]. It can also be used to synthesize the antibiotic (+)-nojirimycin.

CONTACT/Email address: Joy@coreychem.com

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