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Catalog Number:
20486
CAS Number:
101774-27-0
6-Bromo-1H-indole-3-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
6-Bromo-indole-3-carboxylic acid
Documents
$81.92 /250MG
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Product Information

6-Bromo-1H-indole-3-carboxylic acid is a versatile compound widely utilized in pharmaceutical research and organic synthesis. This compound, characterized by its unique bromine substitution, serves as a valuable building block in the development of various bioactive molecules. Its structure allows for significant modifications, making it an essential intermediate in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-inflammatory and anticancer properties. Researchers often leverage this compound in drug discovery processes, particularly in the design of novel therapeutic agents targeting various diseases.

In addition to its applications in medicinal chemistry, 6-Bromo-1H-indole-3-carboxylic acid is also employed in the development of agrochemicals and functional materials. Its ability to undergo various chemical transformations enhances its utility in creating innovative solutions in these fields. The compound's stability and reactivity make it an attractive option for researchers looking to explore new pathways in synthetic chemistry. With its broad range of applications, 6-Bromo-1H-indole-3-carboxylic acid stands out as a key player in advancing both pharmaceutical and agricultural sciences.

Synonyms
6-Bromo-indole-3-carboxylic acid
CAS Number
101774-27-0
Purity
≥ 98% (HPLC)
Molecular Formula
C9H6BrNO2
Molecular Weight
240.06
MDL Number
MFCD05664008
PubChem ID
15284837
Appearance
White or light yellow powder
Conditions
Store at 0-8 °C
General Information
Synonyms
6-Bromo-indole-3-carboxylic acid
CAS Number
101774-27-0
Purity
≥ 98% (HPLC)
Molecular Formula
C9H6BrNO2
Molecular Weight
240.06
MDL Number
MFCD05664008
PubChem ID
15284837
Appearance
White or 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

6-Bromo-1H-indole-3-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly those targeting neurological disorders, enhancing drug efficacy and specificity.
  • Biological Research: It is employed in studies investigating the mechanisms of action of indole derivatives, helping researchers understand their role in cellular processes and disease pathways.
  • Organic Synthesis: The compound is a valuable building block in organic synthesis, allowing chemists to create complex molecules with diverse functional groups, facilitating innovation in material science.
  • Fluorescent Probes: Its unique structure makes it suitable for developing fluorescent probes used in imaging techniques, aiding in the visualization of biological processes in live cells.
  • Environmental Chemistry: Researchers utilize this compound to study its interactions in environmental systems, contributing to the understanding of pollutant behavior and degradation pathways.

Citations