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CAS 198402-60-7

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5-Bromo-6-chloro-1H-indol-3-yl α-D-galactopyranoside

Description:
5-Bromo-6-chloro-1H-indol-3-yl α-D-galactopyranoside is a chemical compound that features a complex structure combining an indole moiety with a galactopyranoside sugar unit. The presence of bromine and chlorine substituents on the indole ring contributes to its unique reactivity and potential biological activity. This compound is often studied for its role in biochemical applications, particularly in the context of glycosylation reactions and as a potential probe in biological systems. The α-D-galactopyranoside portion indicates that the sugar is in the pyranose form and is linked to the indole via a glycosidic bond, which can influence its solubility and interaction with biological targets. The compound may exhibit specific properties such as fluorescence or reactivity with certain enzymes, making it useful in research settings. As with many halogenated compounds, it may also possess antimicrobial or antifungal properties, although specific biological activities would need to be evaluated through experimental studies.
Formula:C14H15BrClNO6
InChI:InChI=1/C14H15BrClNO6/c15-6-1-5-8(2-7(6)16)17-3-9(5)22-14-13(21)12(20)11(19)10(4-18)23-14/h1-3,10-14,17-21H,4H2/t10-,11-,12+,13-,14+/m0/s1
InChI key:InChIKey=CHRVKCMQIZYLNM-HTOAHKCRSA-N
SMILES:O(C=1C=2C(=CC(Cl)=C(Br)C2)NC1)[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O
Synonyms:
  • (2S,3S,4R,5R,6S)-2-[(5-bromo-6-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol
  • 5-Bromo-6-Chloro-3-Indolyl Alpha-D-Galactopyranoside
  • 5-Bromo-6-chloro-1H-indol-3-yl α-<span class="text-smallcaps">D</span>-galactopyranoside
  • 5-Bromo-6-chloro-3-indolyla-D-galactopyranoside
  • Magenta(Tm)-Alpha-D-Gal
  • Magenta(Tm)-Alpha-D-Galactoside
  • Magenta-alpha-gal
  • Rarechem Ah Bs 0010
  • α-<span class="text-smallcaps">D</span>-Galactopyranoside, 5-bromo-6-chloro-1H-indol-3-yl
  • α-D-Galactopyranoside, 5-bromo-6-chloro-1H-indol-3-yl
  • See more synonyms
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