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CAS 1326804-93-6

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4-Methylphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside

Description:
4-Methylphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside is a complex organic compound characterized by its glycosidic structure, which includes a thio linkage and multiple aromatic benzoyl and benzylidene groups. This compound features a glucopyranoside backbone, indicating it is derived from glucose, with modifications that enhance its stability and solubility. The presence of the 4-methylphenyl group contributes to its hydrophobic characteristics, while the benzoyl and benzylidene substituents can influence its reactivity and potential applications in organic synthesis or as a biochemical probe. The thioether functionality may impart unique properties, such as increased nucleophilicity or altered electronic characteristics. This compound is likely to be of interest in medicinal chemistry and materials science due to its structural complexity and potential biological activity. Its CAS number, 1326804-93-6, allows for precise identification in chemical databases and literature. Overall, this compound exemplifies the intricate interplay of functional groups in organic chemistry, leading to diverse applications.
Formula:C34H30O7S
Synonyms:
  • (4AR,6S,7R,8S,8aR)-2-phenyl-6-(p-tolylthio)hexahydropyrano[3,2-d][1,3]dioxine-7,8-diyl dibenzoate
  • 4-Methylphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside
  • β-D-Glucopyranoside, 4-methylphenyl 4,6-O-(phenylmethylene)-1-thio-, 2,3-dibenzoate
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