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CAS 467214-46-6

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6-Chloro-1H-indol-3-yl α-<span class="text-smallcaps">D</span>-glucopyranoside

Description:
6-Chloro-1H-indol-3-yl α-D-glucopyranoside is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a chlorine atom at the 6-position of the indole ring contributes to its unique reactivity and potential biological activity. The α-D-glucopyranoside moiety indicates that this compound is a glycoside, where the indole is linked to a glucose unit in its pyranose form, suggesting potential interactions with biological systems, particularly in glycosylation processes. This compound may exhibit various pharmacological properties, making it of interest in medicinal chemistry and drug development. Its specific characteristics, such as solubility, stability, and reactivity, would depend on the functional groups present and the overall molecular structure. Additionally, the compound's CAS number, 467214-46-6, allows for precise identification in chemical databases, facilitating research and application in various scientific fields.
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-RGDJUOJXSA-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-D-glucopyranoside
  • α-D-Glucopyranoside, 6-chloro-1H-indol-3-yl
  • 6-Chloro-3-indolyla-D-glucopyranoside
  • 6-CHLORO-3-INDOXYL-ALPHA-D-GLUCOPYRANOSIDE USP/EP/BP
  • SALMON(TM)-ALPHA-D-GLUCOSIDE
  • 6-Chloro-3-indoxyl-α-D-glucopyranoside
  • 6-Chloro-3-indolyl alpha-glucopyranoside
  • 6-CHLORO-3-INDOXYL-ALPHA-D-GLUCOPYRANOSIDE
  • SALMON(TM)-ALPHA-D-GLC
  • Salmon alpha-glucoside
  • See more synonyms
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