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Catalog Number:
44388
CAS Number:
13275-42-8
2-(2-Bromophenyl)-1H-benzimidazole
Purity:
≥ 98% (GC)
Synonym(s):
2-(2-Bromophenyl)-1H-1,3-benzodiazole
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Product Information

2-(2-Bromophenyl)-1H-benzimidazole is a versatile compound known for its significant applications in the pharmaceutical and chemical research industries. This compound features a unique structure that allows it to function effectively as a building block in the synthesis of various biologically active molecules. Its bromophenyl group enhances its reactivity, making it a valuable intermediate in the development of novel pharmaceuticals, particularly in the field of anti-cancer and anti-inflammatory agents. Researchers have utilized this compound in the design of targeted therapies, showcasing its potential in medicinal chemistry.

Additionally, 2-(2-Bromophenyl)-1H-benzimidazole exhibits noteworthy properties that make it suitable for use in organic electronics and materials science. Its stability and electronic characteristics allow for applications in the development of organic light-emitting diodes (OLEDs) and other electronic devices. The compound's ability to form stable complexes with various metals also opens avenues for its use in catalysis and coordination chemistry. With its diverse applications and unique properties, this compound is an essential resource for researchers and industry professionals looking to innovate in their respective fields.

Synonyms
2-(2-Bromophenyl)-1H-1,3-benzodiazole
CAS Number
13275-42-8
Purity
≥ 98% (GC)
Molecular Formula
C13H9BrN2
Molecular Weight
273.13
MDL Number
MFCD00449969
PubChem ID
97511
Melting Point
239 - 243 °C
Appearance
White to yellow to orange powder to crystal
Conditions
Store at RT
General Information
Synonyms
2-(2-Bromophenyl)-1H-1,3-benzodiazole
CAS Number
13275-42-8
Purity
≥ 98% (GC)
Molecular Formula
C13H9BrN2
Molecular Weight
273.13
MDL Number
MFCD00449969
PubChem ID
97511
Melting Point
239 - 243 °C
Appearance
White to yellow to orange powder to crystal
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(2-Bromophenyl)-1H-benzimidazole 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 cancer and infectious diseases, due to its ability to interact with biological targets effectively.
  • Research in Biochemistry: It is used in studies investigating enzyme inhibition and receptor binding, providing insights into molecular interactions and potential therapeutic pathways.
  • Material Science: The compound is explored for its properties in developing advanced materials, including organic semiconductors and photonic devices, enhancing performance in electronics.
  • Analytical Chemistry: It acts as a standard reference material in chromatographic methods, aiding in the accurate analysis of complex mixtures in various samples.
  • Environmental Science: This chemical is studied for its behavior and degradation in environmental matrices, contributing to assessments of chemical safety and impact on ecosystems.

Citations