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CAS 25577-40-6

:

a-D-Glucopyranoside, methyl4,6-O-(phenylmethylene)-, 2-acetate

Description:
α-D-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, 2-acetate, with the CAS number 25577-40-6, is a glycoside derivative of glucose. This compound features a glucopyranoside structure, which is a six-membered cyclic form of glucose, and is modified with a methoxy group and a phenylmethylene group at the 4 and 6 positions, respectively. Additionally, it has an acetate group at the 2-position, which contributes to its reactivity and solubility characteristics. The presence of the phenylmethylene moiety enhances its hydrophobic properties, potentially influencing its interactions in biological systems. This compound may exhibit various chemical properties, including solubility in organic solvents and potential reactivity in glycosylation reactions. Its structural modifications suggest potential applications in organic synthesis, particularly in the development of glycosylated compounds for pharmaceutical or biochemical research. As with many glycosides, it may also exhibit specific biological activities, although detailed studies would be necessary to elucidate its full range of properties and applications.
Formula:C16H20O7
Synonyms:
  • Glucopyranoside,methyl 4,6-O-benzylidene-, 2-acetate (7CI)
  • Glucopyranoside, methyl4,6-O-benzylidene-, 2-acetate, a-D- (8CI)
  • a-D-Glucopyranoside,methyl 4,6-O-benzylidene-, 2-acetate (6CI)
  • Pyrano[3,2-d]-1,3-dioxin, a-D-glucopyranoside deriv.
  • Methyl2-O-acetyl-4,6-O-benzylidene-a-D-glucopyranoside
  • Methyl 2-O-acetyl-4,6-O-benzylidene-alpha-D-glucopyranoside
  • α-D-Glucopyranoside, methyl 4,6-O-(phenylmethylene)-, 2-acetate
  • Methyl 2-O-acetyl-4,6-O-benzylidene-a-D-glucopyranoside
  • Methyl 2-O-acetyl-4,6-O-benzylidene-α-D-glucopyranoside
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