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Catalog Number:
21001
CAS Number:
125229-64-3
5-Bromo-4-chloro-3-indolyl α-D-mannopyranoside
Synonym(s):
X-α-D-mannoside
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Product Information

5-Bromo-4-chloro-3-indolyl a-D-mannopyranoside is a versatile compound widely utilized in biochemical research and various industrial applications. This compound serves as a valuable substrate in enzyme assays, particularly for studying glycosidases and other carbohydrate-active enzymes. Its unique structure, featuring both bromine and chlorine substituents, enhances its reactivity and makes it an excellent choice for probing enzyme specificity and activity. Researchers appreciate its ability to provide clear and quantifiable results, facilitating advancements in carbohydrate chemistry and enzymology.

In addition to its applications in enzyme studies, 5-Bromo-4-chloro-3-indolyl a-D-mannopyranoside is also employed in the synthesis of complex carbohydrates and glycosides, contributing to the development of novel pharmaceuticals and bioactive compounds. Its stability and reactivity under various conditions make it a preferred choice for researchers looking to explore the intricate interactions of carbohydrates in biological systems. With its broad range of applications and significant benefits, this compound is an essential tool for professionals in the fields of biochemistry, molecular biology, and pharmaceutical development.

Synonyms
X-α-D-mannoside
CAS Number
125229-64-3
Molecular Formula
C14H15BrClNO6
Molecular Weight
408.63
MDL Number
MFCD00078951
PubChem ID
619018
Conditions
Store at 0-8°C
General Information
Synonyms
X-α-D-mannoside
CAS Number
125229-64-3
Molecular Formula
C14H15BrClNO6
Molecular Weight
408.63
MDL Number
MFCD00078951
PubChem ID
619018
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

5-Bromo-4-chloro-3-indolyl a-D-mannopyranoside is widely utilized in research focused on:

  • Biochemical Assays: This compound serves as a substrate in enzyme assays, particularly for studying glycosidases, which are crucial in various metabolic processes.
  • Plant Research: It is employed in plant biology to investigate the mechanisms of carbohydrate metabolism and the role of indole derivatives in plant growth and development.
  • Drug Development: The compound is explored in pharmaceutical research for its potential as a lead compound in developing new drugs targeting specific biological pathways.
  • Fluorescent Probes: It can be used to create fluorescent probes for imaging studies, helping researchers visualize cellular processes in real-time.
  • Food Industry: This chemical finds applications in food science for studying the effects of glycosylation on flavor compounds and food preservation techniques.

Citations