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CAS 125229-64-3

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5-bromo-4-chloro-3-indolyl A-D-*mannopyranoside

Description:
5-Bromo-4-chloro-3-indolyl A-D-mannopyranoside is a synthetic compound often used in biochemical research, particularly in the study of glycosidases and glycosylation processes. This compound features a chromogenic indole moiety, which allows for colorimetric detection, making it valuable in assays for enzyme activity. The presence of bromine and chlorine substituents on the indole ring enhances its reactivity and specificity in biochemical applications. The mannopyranoside part of the molecule indicates that it is a glycoside derived from mannose, a six-carbon sugar, which can influence its solubility and interaction with biological systems. This compound is typically used in laboratory settings and may require careful handling due to its halogenated nature, which can pose environmental and health risks. Its applications extend to molecular biology, where it serves as a substrate for studying enzyme kinetics and mechanisms. Overall, 5-bromo-4-chloro-3-indolyl A-D-mannopyranoside is a versatile tool in the field of enzymology and carbohydrate chemistry.
Formula:C14H15BrClNO6
InChI:InChI=1/C14H15BrClNO6/c15-5-1-2-6-9(10(5)16)7(3-17-6)22-14-13(21)12(20)11(19)8(4-18)23-14/h1-3,8,11-14,17-21H,4H2/t8-,11-,12+,13+,14+/m1/s1
Synonyms:
  • 5-Bromo-4-chloro-3-indolyl-ALPHA-D-mannopyranoside
  • 5-bromo-4-chloro-1H-indol-3-yl hexopyranoside
  • 5-bromo-4-chloro-1H-indol-3-yl alpha-D-mannopyranoside
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