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CAS 3150-15-0

:

Methyl 2,3-anhydro-4,6-O-(phenylmethylene)-α-D-allopyranoside

Description:
Methyl 2,3-anhydro-4,6-O-(phenylmethylene)-α-D-allopyranoside, with the CAS number 3150-15-0, is a carbohydrate derivative characterized by its anhydro sugar structure. This compound features a methyl ether group, which enhances its solubility in organic solvents. The presence of the phenylmethylene group contributes to its aromatic characteristics, potentially influencing its reactivity and interaction with other molecules. The anhydro configuration indicates that it has undergone a dehydration reaction, which can affect its stability and reactivity in various chemical environments. This compound is typically used in organic synthesis and may serve as an intermediate in the preparation of more complex molecules. Its structural features suggest potential applications in medicinal chemistry and materials science, particularly in the development of glycosylated compounds or as a building block for more complex carbohydrate structures. As with many organic compounds, handling should be done with care, considering its chemical properties and potential reactivity.
Formula:C14H16O5
InChI:InChI=1S/C14H16O5/c1-15-14-12-11(18-12)10-9(17-14)7-16-13(19-10)8-5-3-2-4-6-8/h2-6,9-14H,7H2,1H3/t9-,10-,11-,12-,13?,14+/m1/s1
InChI key:InChIKey=HQTCRHINASMQOA-BTZLDLHRSA-N
SMILES:O(C)[C@@H]1[C@]2([C@@]([C@]3([C@](O1)(COC(O3)C4=CC=CC=C4)[H])[H])(O2)[H])[H]
Synonyms:
  • Methyl 2,3-anhydro-4,6-O-(phenylmethylene)-α-D-allopyranoside
  • Oxireno[4,5]pyrano[3,2-d][1,3]dioxin, α-D-allopyranoside deriv.
  • Methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside
  • Allopyranoside, methyl 2,3-anhydro-4,6-O-benzylidene-, α-D-
  • α-D-Allopyranoside, methyl 2,3-anhydro-4,6-O-(phenylmethylene)-
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