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CAS 1210344-58-3

:

1,6-Anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-5-C-(hydroxymethyl)-β-<span class="text-smallcaps">L</span>-gulopyranose

Description:
1,6-Anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-5-C-(hydroxymethyl)-β-L-gulopyranose is a complex organic compound characterized by its unique structural features. It contains a pyranose ring, which is a six-membered cyclic structure typical of sugars, specifically in the β-anomeric configuration. The presence of an anhydro group indicates that it has undergone dehydration, resulting in a ring structure that lacks a hydroxyl group at the anomeric carbon. The compound also features a chlorinated phenyl group and an ethoxy-substituted phenyl moiety, which contribute to its potential biological activity and solubility properties. The hydroxymethyl group at the 5-position of the sugar ring enhances its reactivity and may influence its interactions in biological systems. Overall, this compound's intricate structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or as a biochemical probe, although specific biological activities would require further investigation.
Formula:C22H25ClO7
InChI:InChI=1S/C22H25ClO7/c1-2-28-16-6-3-13(4-7-16)9-14-10-15(5-8-17(14)23)22-20(27)18(25)19(26)21(11-24,30-22)12-29-22/h3-8,10,18-20,24-27H,2,9,11-12H2,1H3/t18-,19-,20-,21-,22-/m0/s1
InChI key:InChIKey=MCIACXAZCBVDEE-YFNVTMOMSA-N
SMILES:O[C@@H]1[C@@]2(O[C@@](CO)(CO2)[C@@H](O)[C@@H]1O)C3=CC(CC4=CC=C(OCC)C=C4)=C(Cl)C=C3
Synonyms:
  • 1,6-Anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-5-C-(hydroxymethyl)-β-L-gulopyranose
  • β-L-Gulopyranose, 1,6-anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-5-C-(hydroxymethyl)-
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