CAS 13322-90-2

3,4,6-Tri-O-benzoyl-D-glucal, 97%

Description:

3,4,6-Tri-O-benzoyl-D-glucal is a chemical compound that serves as a derivative of D-glucose, characterized by the presence of three benzoyl groups attached to the hydroxyl positions at carbons 3, 4, and 6. This modification enhances its lipophilicity and stability, making it useful in organic synthesis and carbohydrate chemistry. The compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and ethyl acetate, but less soluble in water due to its hydrophobic nature. It is often utilized as a glycosyl donor in glycosylation reactions, facilitating the formation of glycosidic bonds in the synthesis of oligosaccharides and complex carbohydrates. The purity of 97% indicates a high level of refinement, making it suitable for research and industrial applications. As with many organic compounds, proper handling and storage are essential to maintain its integrity and prevent degradation. Safety data sheets should be consulted for information on hazards and safe handling practices.

Formula: C₂₇H₂₂O₇

Synonyms:

• TRI-O-BENZOYL-D-GLUCAL
• D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-, 3,4,6-tribenzoate
• 3,4,6-Tri-O-benzoyl-D-glucal, 97%

3,4,6-Tri-O-benzoyl-D-glucal, 97%

CAS: 13322-90-2

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₂₇H₂₂O₇

Purity: 97%

Molecular weight: 458.46

Ref: 02-H60637

3,4,6-Tri-O-benzoyl-D-glucal

CAS: 13322-90-2

Formula: C₂₇H₂₂O₇

Purity: 95%

Molecular weight: 458.4594

Ref: IN-DA009IKG

3,4,6-Tri-o-benzoyl-D-glucal

CAS: 13322-90-2

3,4,6-Tri-o-benzoyl-D-glucal is a glycoside that is synthesized by the reaction of 3,4,6-tri-O-benzoyl D-glucose with nitrate. This synthesis yields a mixture of three stereoisomers: erythro-, threo-, and erythro-. The erythro stereoisomer has been shown to be more active than the threo and erythro stereoisomers. The use of catalytic amounts of alcohols and acetonitrile in this reaction leads to the formation of c0glycosides. Ammonium nitrate is used as an oxidant in this type of reaction and can be used as a reducing agent or reagent for hydrolysis.

Formula: C₂₇H₂₂O₇

Purity: Min. 95%

Molecular weight: 458.5 g/mol

Ref: 3D-NAA32290