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CAS 14125-75-8

:

1,5-Anhydro-D-arabino-hex-1-enitol 2,3,4,6-tetrabenzoate

Description:
1,5-Anhydro-D-arabino-hex-1-enitol 2,3,4,6-tetrabenzoate is a chemical compound characterized by its complex structure, which includes multiple benzoyl groups attached to a sugar derivative. This compound is a derivative of a sugar alcohol, specifically an anhydro form of D-arabino-hex-1-enitol, indicating that it has undergone dehydration to form a cyclic structure. The presence of four benzoyl groups suggests that it has significant hydrophobic characteristics, which can influence its solubility and reactivity. The tetrabenzoate moiety may enhance its stability and alter its interaction with biological systems, making it of interest in various fields, including medicinal chemistry and materials science. Additionally, the compound may exhibit unique optical properties due to its chiral centers, which can be relevant in applications involving stereochemistry. Overall, 1,5-Anhydro-D-arabino-hex-1-enitol 2,3,4,6-tetrabenzoate is notable for its structural complexity and potential applications in organic synthesis and pharmaceutical development.
Formula:C34H26O9
InChI:InChI=1S/C34H26O9/c35-31(23-13-5-1-6-14-23)40-21-27-29(42-33(37)25-17-9-3-10-18-25)30(43-34(38)26-19-11-4-12-20-26)28(22-39-27)41-32(36)24-15-7-2-8-16-24/h1-20,22,27,29-30H,21H2/t27-,29-,30-/m1/s1
InChI key:InChIKey=HHNQKUIYTNDYHW-MJLPRTPSSA-N
SMILES:O(C(=O)C1=CC=CC=C1)[C@H]2[C@H](OC(=O)C3=CC=CC=C3)[C@@H](COC(=O)C4=CC=CC=C4)OC=C2OC(=O)C5=CC=CC=C5
Synonyms:
  • D-arabino-Hex-1-enopyranose, 1-deoxy-, tetrabenzoate
  • Glucal, 2-hydroxy-, tetrabenzoate
  • D-arabino-Hex-1-enitol, 1,5-anhydro-, tetrabenzoate
  • D-arabino-Hex-1-enitol, 1,5-anhydro-, 2,3,4,6-tetrabenzoate
  • 1,5-Anhydro-D-arabino-hex-1-enitol 2,3,4,6-tetrabenzoate
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