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Catalog Number:
21839
CAS Number:
7254-19-5
5-Bromoindole-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
5-Bromo-1H-indole-2-carboxylic acid
Documents
$22.03 /1G
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Product Information

5-Bromoindole-2-carboxylic acid is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This compound, characterized by its bromine substitution at the 5-position of the indole ring, exhibits unique reactivity that makes it an essential building block for the development of various pharmaceuticals and agrochemicals. Its carboxylic acid functionality enhances its solubility and reactivity, allowing for straightforward incorporation into complex molecular architectures.

Researchers have leveraged 5-Bromoindole-2-carboxylic acid in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-cancer and anti-inflammatory properties. Additionally, its application extends to the development of novel materials and dyes, showcasing its potential in various industrial applications. The compound's ability to participate in coupling reactions further enhances its utility, making it a valuable asset for both academic and industrial chemists seeking to innovate in drug discovery and material science.

Synonyms
5-Bromo-1H-indole-2-carboxylic acid
CAS Number
7254-19-5
Purity
≥ 98% (HPLC)
Molecular Formula
C9H6BrNO2
Molecular Weight
240.06
MDL Number
MFCD00022705
PubChem ID
252137
Appearance
Light yellow powder
Conditions
Store at 0-8°C
General Information
Synonyms
5-Bromo-1H-indole-2-carboxylic acid
CAS Number
7254-19-5
Purity
≥ 98% (HPLC)
Molecular Formula
C9H6BrNO2
Molecular Weight
240.06
MDL Number
MFCD00022705
PubChem ID
252137
Appearance
Light yellow 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-Bromoindole-2-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with serotonin receptors.
  • Biochemical Research: It is often used in studies related to protein interactions and enzyme activity, helping researchers understand cellular processes and develop new therapeutic strategies.
  • Material Science: The compound is explored in the development of advanced materials, such as organic semiconductors, due to its unique electronic properties.
  • Agrochemical Applications: It has potential uses in the formulation of agrochemicals, contributing to the development of more effective and environmentally friendly pesticides.
  • Fluorescent Probes: 5-Bromoindole-2-carboxylic acid is employed in creating fluorescent probes for imaging studies, enhancing the ability to visualize biological processes in real-time.

Citations