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Catalog Number:
20998
CAS Number:
125328-76-9
5-Bromo-4-chloro-3-indoxyl-1-acétate
Purity:
≥ 99% (GC)
Synonym(s):
1-Acétyl-5-bromo-4-chloro-1 H -indol-3-ol, N -Acétyl-5-bromo-4-chloro-3-hydroxy-1 H -indole
Documents
$117.78 /100 mg
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Product Information

5-Bromo-4-chloro-3-indoxyl-1-acetate is a versatile chemical compound widely utilized in biochemical research and various industrial applications. This compound serves as a substrate for the enzyme β-galactosidase, making it invaluable in molecular biology for detecting enzyme activity. Its ability to produce a colored product upon enzymatic hydrolysis allows researchers to visualize and quantify enzyme activity in a straightforward manner, facilitating studies in gene expression and cellular processes. Additionally, its unique structure contributes to its effectiveness in histochemical staining, providing clear and distinct results in tissue samples.

In the pharmaceutical industry, 5-Bromo-4-chloro-3-indoxyl-1-acetate is also explored for its potential applications in drug development and testing. Its properties enable researchers to investigate various biochemical pathways and interactions, making it a crucial tool in the development of new therapeutic agents. The compound's stability and ease of use further enhance its appeal, ensuring reliable results in both laboratory and industrial settings.

Synonyms
1-Acétyl-5-bromo-4-chloro-1 H -indol-3-ol, N -Acétyl-5-bromo-4-chloro-3-hydroxy-1 H -indole
CAS Number
125328-76-9
Purity
≥ 99% (GC)
Molecular Formula
C10H7BrClNO2
Molecular Weight
288.53
MDL Number
MFCD04972041
PubChem ID
17955304
Melting Point
171-175 ?C
Appearance
Poudre jaunâtre
Conditions
Conserver à 0-8 °C
General Information
Synonyms
1-Acétyl-5-bromo-4-chloro-1 H -indol-3-ol, N -Acétyl-5-bromo-4-chloro-3-hydroxy-1 H -indole
CAS Number
125328-76-9
Purity
≥ 99% (GC)
Molecular Formula
C10H7BrClNO2
Molecular Weight
288.53
MDL Number
MFCD04972041
PubChem ID
17955304
Melting Point
171-175 ?C
Appearance
Poudre jaunâtre
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Bromo-4-chloro-3-indoxyl-1-acetate is widely utilized in research focused on:

  • Histochemical Staining: This compound is commonly used as a substrate in histochemical assays, allowing researchers to visualize enzyme activity in tissues, which is crucial for studying various biological processes.
  • Biochemical Research: It serves as a valuable tool for studying the activity of specific enzymes, particularly in the field of molecular biology, helping scientists understand metabolic pathways and enzyme kinetics.
  • Plant Research: In plant biology, it is used to investigate gene expression and the effects of various treatments on plant tissues, aiding in the development of genetically modified crops.
  • Diagnostic Applications: This compound has potential uses in developing diagnostic tests, particularly in identifying certain pathogens or conditions based on enzyme activity, enhancing the accuracy of medical diagnostics.
  • Pharmaceutical Development: It plays a role in drug discovery processes, particularly in screening for compounds that can inhibit or activate specific biological targets, streamlining the development of new therapeutics.

Citations