CAS 17791-36-5
:METHYL 2,3-DI-O-BENZYL-ALPHA-D-GLUCOPYRANOSIDE
Description:
Methyl 2,3-di-O-benzyl-alpha-D-glucopyranoside is a glycoside derivative of glucose, characterized by the presence of two benzyl groups attached to the 2 and 3 positions of the glucopyranose ring, along with a methoxy group at the anomeric carbon. This compound is typically a white to off-white crystalline solid, exhibiting moderate solubility in organic solvents such as methanol and dichloromethane, while being less soluble in water due to its hydrophobic benzyl substituents. It is often used in organic synthesis and carbohydrate chemistry as a protecting group for hydroxyl functionalities, facilitating further chemical transformations. The presence of the benzyl groups enhances its stability and reactivity, making it a valuable intermediate in the synthesis of more complex carbohydrates and glycosides. Additionally, its structural features may influence its biological activity, making it of interest in medicinal chemistry and pharmacology. Proper handling and storage conditions should be observed, as with many organic compounds, to ensure safety and maintain compound integrity.
Formula:C21H26O6
InChI:InChI=1/C21H26O6/c1-24-21-20(26-14-16-10-6-3-7-11-16)19(18(23)17(12-22)27-21)25-13-15-8-4-2-5-9-15/h2-11,17-23H,12-14H2,1H3
SMILES:COC1C(C(C(C(CO)O1)O)OCc1ccccc1)OCc1ccccc1
Synonyms:- methyl 2,3-di-O-benzylhexopyranoside
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Found 3 products.
Methyl 2,3-di-O-benzyl-α-D-glucopyranoside
CAS:<p>Methyl 2,3-di-O-benzyl-α-D-glucopyranoside</p>Molecular weight:374.42754g/molMethyl 2,3-di-O-benzyl-α-D-glucopyranoside
CAS:<p>Methyl 2,3-di-O-benzyl-a-D-glucopyranoside is a chiral sugar that can be synthesized by sulfidation of methyl 1,2,3,4-tetra-O-benzyloxycarbonyl-a-D-glucopyranoside. This sugar was used in the synthesis of oxathianes and sulfones as well as other synthetic methodology.</p>Formula:C21H26O6Purity:Min. 95%Color and Shape:PowderMolecular weight:374.43 g/mol
