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Catalog Number:
29970
CAS Number:
3030-06-6
5-Bromo-4-chloroindoxyl 1,3-diacetate
Purity:
≥ 99% (HPLC)
Synonym(s):
5-Bromo-4-chloro-3-indolyl-1,3-diacetate
Documents
$51.18 /1G
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Product Information

5-Bromo-4-chloro-3-indolyl-1,3-diacetate is a versatile compound widely utilized in biochemical research and pharmaceutical applications. This compound is recognized for its role as a substrate in various enzymatic assays, particularly in studies involving β-glucuronidase and other glycosyltransferases. Its unique structure allows for effective tagging and detection in biological systems, making it an essential tool for researchers investigating metabolic pathways and enzyme activities. Additionally, the compound's bromine and chlorine substituents enhance its reactivity, enabling the synthesis of more complex molecules, which can be pivotal in drug development and chemical biology.

The practical applications of 5-Bromo-4-chloro-3-indolyl-1,3-diacetate extend to its use in the development of colorimetric assays, where it serves as a chromogenic substrate. This property is particularly beneficial in diagnostic applications, allowing for the visual detection of enzymatic activity. Researchers and industry professionals can leverage this compound to streamline their experimental processes, improve assay sensitivity, and enhance the overall efficiency of their studies. Its compatibility with various biological systems further underscores its importance in both academic and industrial settings.

Synonyms
5-Bromo-4-chloro-3-indolyl-1,3-diacetate
CAS Number
3030-06-6
Purity
≥ 99% (HPLC)
Molecular Formula
C12H9BrClNO3
Molecular Weight
330.56
MDL Number
MFCD00040632
PubChem ID
76416
Melting Point
165 - 168 ?C
Appearance
Yellow to yellowish brown powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
5-Bromo-4-chloro-3-indolyl-1,3-diacetate
CAS Number
3030-06-6
Purity
≥ 99% (HPLC)
Molecular Formula
C12H9BrClNO3
Molecular Weight
330.56
MDL Number
MFCD00040632
PubChem ID
76416
Melting Point
165 - 168 ?C
Appearance
Yellow to yellowish brown powder
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-1,3-diacetate is widely utilized in research focused on:

  • Biological Research: This compound serves as a substrate in enzyme assays, particularly for studying β-glucuronidase activity, which is important in pharmacokinetics and drug metabolism studies.
  • Histochemical Staining: It is used in histology for staining tissues, allowing researchers to visualize specific cellular components, enhancing the understanding of various diseases.
  • Pharmaceutical Development: The compound plays a role in the synthesis of indole derivatives, which are crucial in developing new drugs, particularly in oncology and anti-inflammatory therapies.
  • Environmental Monitoring: It can be employed in assays to detect environmental pollutants, aiding in the assessment of soil and water quality.
  • Material Science: This chemical is explored in the development of new materials, such as organic semiconductors, which have applications in electronics and photonics.

Citations