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CAS 425427-88-9

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6-Chloro-1H-indol-3-yl α-D-mannopyranoside

Description:
6-Chloro-1H-indol-3-yl α-D-mannopyranoside is a chemical compound characterized by its unique structure, which combines an indole moiety with a mannopyranoside sugar unit. The presence of the chloro group at the 6-position of the indole ring contributes to its reactivity and potential biological activity. This compound is typically used in biochemical research, particularly in studies related to glycosylation and the interaction of indole derivatives with biological systems. Its α-D-mannopyranoside configuration suggests that it can participate in glycosidic bond formation, making it relevant in the synthesis of glycosylated compounds. The compound's solubility and stability can vary depending on the solvent and conditions used, which is important for its application in laboratory settings. Additionally, due to the indole structure, it may exhibit fluorescence properties, making it useful in various analytical techniques. Overall, 6-Chloro-1H-indol-3-yl α-D-mannopyranoside is a valuable compound in organic and medicinal chemistry, with potential implications in drug development and biochemical research.
Formula:C14H16ClNO6
InChI:InChI=1S/C14H16ClNO6/c15-6-1-2-7-8(3-6)16-4-9(7)21-14-13(20)12(19)11(18)10(5-17)22-14/h1-4,10-14,16-20H,5H2/t10-,11-,12+,13+,14+/m1/s1
InChI key:InChIKey=OQWBAXBVBGNSPW-DGTMBMJNSA-N
SMILES:O(C=1C=2C(NC1)=CC(Cl)=CC2)[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]3O
Synonyms:
  • 6-Chloro-1H-indol-3-yl α-<span class="text-smallcaps">D</span>-mannopyranoside
  • 6-Chloro-3-Indolyl Alpha-D-Mannopyranoside
  • 6-Chloro-3-Indoxyl-Alpha-D-Mannopyranoside
  • 6-Chloro-3-indolyla-D-mannopyranoside
  • Rarechem Ah Bs 0032
  • Rose(Tm)-Alpha-Mannoside
  • Salmon(Tm)-Alpha-D-Man
  • Salmon(Tm)-Alpha-D-Mannoside
  • Salmon-alpha-mannoside
  • α-<span class="text-smallcaps">D</span>-Mannopyranoside, 6-chloro-1H-indol-3-yl
  • See more synonyms
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