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Catalog Number:
17701
CAS Number:
16694-17-0
4-Bromo-thiophene-3-carboxylic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
4-Bromo-3-thiophenecarboxylic acid
Documents
$45.47 /250MG
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Product Information

4-Bromo-thiophene-3-carboxylic acid is a versatile compound widely utilized in organic synthesis and materials science. This aromatic carboxylic acid features a bromine substituent that enhances its reactivity, making it an excellent building block for the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its unique thiophene ring structure provides distinct electronic properties, which are beneficial in the development of organic semiconductors and conductive polymers. Researchers have effectively employed this compound in the creation of novel dyes and sensors, showcasing its potential in advanced electronic applications.

In addition to its synthetic utility, 4-Bromo-thiophene-3-carboxylic acid is recognized for its role in the development of biologically active compounds. Its ability to participate in cross-coupling reactions allows for the formation of complex molecular architectures, making it a valuable tool for medicinal chemists. With its favorable properties and diverse applications, this compound stands out as a key ingredient in the ongoing innovation within the chemical and pharmaceutical industries.

Synonyms
4-Bromo-3-thiophenecarboxylic acid
CAS Number
16694-17-0
Purity
≥ 95% (HPLC)
Molecular Formula
C5H3BrO2S
Molecular Weight
207.05
MDL Number
MFCD01233020
PubChem ID
85546
Appearance
White to yellow solid
Conditions
Store at 0-8°C
General Information
Synonyms
4-Bromo-3-thiophenecarboxylic acid
CAS Number
16694-17-0
Purity
≥ 95% (HPLC)
Molecular Formula
C5H3BrO2S
Molecular Weight
207.05
MDL Number
MFCD01233020
PubChem ID
85546
Appearance
White to yellow solid
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

4-Bromo-thiophene-3-carboxylic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Material Science: It is used in the production of conductive polymers and materials, enhancing the performance of electronic devices such as organic light-emitting diodes (OLEDs).
  • Medicinal Chemistry: Researchers leverage its properties to design and develop new drugs, particularly those targeting specific biological pathways due to its unique structural features.
  • Analytical Chemistry: This compound is utilized as a standard in chromatographic methods, aiding in the analysis and quantification of related compounds in various samples.
  • Environmental Science: It plays a role in the study of environmental pollutants, helping scientists understand the behavior and degradation of thiophene derivatives in ecosystems.

Citations