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CAS 40983-94-6

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Phenylmethyl 4,6-O-(phenylmethylene)-α-D-mannopyranoside

Description:
Phenylmethyl 4,6-O-(phenylmethylene)-α-D-mannopyranoside, with the CAS number 40983-94-6, is a glycoside derivative of mannose, characterized by the presence of a phenylmethyl group and a phenylmethylene moiety. This compound features a pyranose ring structure, which is typical of many sugars, and the specific substitution patterns contribute to its unique chemical properties. It is generally soluble in organic solvents and may exhibit limited solubility in water due to its hydrophobic phenyl groups. The presence of multiple aromatic rings can influence its reactivity, stability, and potential interactions with biological systems. This compound may be of interest in various fields, including organic synthesis and medicinal chemistry, due to its potential biological activities and applications in drug development. Its structural complexity and functional groups may also allow for further modifications, making it a versatile candidate for research in carbohydrate chemistry and related disciplines.
Formula:C20H22O6
InChI:InChI=1S/C20H22O6/c21-16-17(22)20(23-11-13-7-3-1-4-8-13)25-15-12-24-19(26-18(15)16)14-9-5-2-6-10-14/h1-10,15-22H,11-12H2/t15-,16-,17+,18-,19?,20+/m1/s1
InChI key:InChIKey=LEJLVYJUXVHIJN-LOZDCHMLSA-N
SMILES:O[C@H]1[C@]2([C@](O[C@H](OCC3=CC=CC=C3)[C@H]1O)(COC(O2)C4=CC=CC=C4)[H])[H]
Synonyms:
  • α-D-Mannopyranoside, phenylmethyl 4,6-O-(phenylmethylene)-
  • Pyrano[3,2-d]-1,3-dioxin, α-D-mannopyranoside deriv.
  • Phenylmethyl 4,6-O-(phenylmethylene)-α-D-mannopyranoside
  • Benzyl 4,6-O-benzylidene-α-D-mannopyranoside
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