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Catalog Number:
03558
CAS Number:
129541-43-1
5-Bromo-4-chloro-3-indolyl butyrate
Purity:
≥ 99% (TLC)
Synonym(s):
5-Bromo-4-chloroindoxylbutyrate
Documents
$51.18 /100MG
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Product Information

5-Bromo-4-chloro-3-indolyl butyrate is a versatile compound widely recognized for its applications in biochemical research and pharmaceutical development. This compound serves as a substrate for various enzymatic reactions, particularly in studies involving the activity of esterases and lipases. Its unique structure, featuring both bromine and chlorine substituents, enhances its reactivity and makes it an excellent candidate for probing metabolic pathways. Researchers utilize 5-Bromo-4-chloro-3-indolyl butyrate in the development of assays for drug discovery, particularly in the evaluation of enzyme inhibitors and activators, providing valuable insights into therapeutic targets.

In addition to its research applications, this compound has potential uses in the synthesis of novel indole derivatives, which are important in medicinal chemistry due to their diverse biological activities. The ability to modify its structure allows for the exploration of new compounds with enhanced efficacy and specificity. With its robust profile, 5-Bromo-4-chloro-3-indolyl butyrate stands out as a key reagent for researchers aiming to advance their studies in enzymology and drug development.

Synonyms
5-Bromo-4-chloroindoxylbutyrate
CAS Number
129541-43-1
Purity
≥ 99% (TLC)
Molecular Formula
C12H11NO2BrCl
Molecular Weight
316.6
MDL Number
MFCD00083261
PubChem ID
688404
Melting Point
90-94 ?C
Appearance
White powder
Conditions
Store at ≤ -15 °C
General Information
Synonyms
5-Bromo-4-chloroindoxylbutyrate
CAS Number
129541-43-1
Purity
≥ 99% (TLC)
Molecular Formula
C12H11NO2BrCl
Molecular Weight
316.6
MDL Number
MFCD00083261
PubChem ID
688404
Melting Point
90-94 ?C
Appearance
White powder
Conditions
Store at ≤ -15 °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 butyrate is widely utilized in research focused on:

  • Biochemical Assays: This compound is commonly used as a substrate in enzyme assays, particularly for studying the activity of esterases and other hydrolases, providing insights into enzyme kinetics and mechanisms.
  • Drug Development: It serves as a valuable tool in pharmaceutical research, aiding in the discovery and optimization of new drug candidates, especially those targeting cancer and other diseases.
  • Cell Biology: Researchers employ this compound to investigate cellular processes, such as apoptosis and differentiation, by monitoring its effects on various cell lines, thus enhancing understanding of cellular behavior.
  • Genetic Studies: It is utilized in genetic research to study gene expression and regulation, particularly in the context of signaling pathways, helping to elucidate the roles of specific genes in disease.
  • Environmental Science: The compound is also explored for its potential applications in environmental monitoring, particularly in assessing the impact of pollutants on biological systems, contributing to ecological research.

Citations