CAS 64768-20-3
:[(2R,3R,4S,5R)-3,4,5-tribenzoyloxy-6-hydroxy-tetrahydropyran-2-yl]methyl benzoate
Description:
The chemical substance with the name "[(2R,3R,4S,5R)-3,4,5-tribenzoyloxy-6-hydroxy-tetrahydropyran-2-yl]methyl benzoate" and CAS number 64768-20-3 is a complex organic compound characterized by its tetrahydropyran ring structure, which is a six-membered cyclic ether. This compound features multiple benzoyloxy groups, indicating the presence of ester functionalities derived from benzoic acid, contributing to its potential applications in organic synthesis and medicinal chemistry. The stereochemistry, denoted by the R and S configurations, suggests specific spatial arrangements of the substituents, which can influence the compound's reactivity and biological activity. The presence of a hydroxy group enhances its polarity and may participate in hydrogen bonding, affecting solubility and interaction with biological targets. Overall, this compound's unique structural features make it of interest for further research in fields such as drug development and materials science, where the manipulation of stereochemistry and functional groups can lead to novel properties and applications.
Formula:C34H28O10
InChI:InChI=1/C34H28O10/c35-30(22-13-5-1-6-14-22)40-21-26-27(42-31(36)23-15-7-2-8-16-23)28(43-32(37)24-17-9-3-10-18-24)29(34(39)41-26)44-33(38)25-19-11-4-12-20-25/h1-20,26-29,34,39H,21H2/t26-,27-,28+,29-,34u/m1/s1
Synonyms:- 2,3,4,6-Tetra-O-benzoyl-D-glucopyranose
- D-glucopyranose, 2,3,4,6-tetrabenzoate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
b-D-Glucopyranose, 2,3,4,6-tetrabenzoate
CAS:Formula:C34H28O10Purity:97%Color and Shape:SolidMolecular weight:596.58012,3,4,6-Tetra-O-benzoyl-β-D-glucopyranose
CAS:<p>2,3,4,6-Tetra-O-benzoyl-β-D-glucopyranose is a D-glucopyranose derivative that has been used in glucosylation reactions.</p>Formula:C34H28O10Color and Shape:SolidMolecular weight:596.582,3,4,6-Tetra-O-benzoyl-D-glucopyranose
CAS:<p>2,3,4,6-Tetra-O-benzoyl-D-glucopyranose is an aldehyde that has been synthesized by the oxidation of D-glucofuranose with nitric acid. It has been shown to act as a competitive inhibitor of lipase and c-glycosidases. The acetal group in 2,3,4,6-tetra-O-benzoyl-D-glucopyranose is activated with acetyl chloride to form an acetal derivative. This compound can be used as a chemoenzymatic glycosidic bond formation method for the synthesis of various glycosides.</p>Formula:C34H28O10Purity:Min. 95%Molecular weight:596.6 g/mol



