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Catalog Number:
26948
CAS Number:
88-13-1
Thiophene-3-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
3-Thenoic acid, 3-Thiophenoic acid
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Product Information

Thiophene-3-carboxylic acid is a versatile heterocyclic compound known for its unique sulfur-containing aromatic structure, which enhances its reactivity and potential applications in various fields. This compound serves as a valuable building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. Its carboxylic acid functional group allows for easy derivatization, making it suitable for creating a wide range of derivatives that can be tailored for specific applications. Researchers have utilized thiophene-3-carboxylic acid in the synthesis of biologically active compounds, including anti-inflammatory agents and antimicrobial substances, showcasing its relevance in medicinal chemistry.

In addition to its pharmaceutical applications, thiophene-3-carboxylic acid is also employed in the production of conductive polymers and organic semiconductors, which are essential in the development of electronic devices. Its ability to participate in various chemical reactions, such as esterification and amidation, further expands its utility in material science. With its unique properties and diverse applications, thiophene-3-carboxylic acid stands out as a crucial compound for researchers and industry professionals seeking innovative solutions in their respective fields.

Synonyms
3-Thenoic acid, 3-Thiophenoic acid
CAS Number
88-13-1
Purity
≥ 98% (HPLC)
Molecular Formula
C5H4O2S
Molecular Weight
128.15
MDL Number
MFCD00005467
PubChem ID
6918
Melting Point
130-145 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
3-Thenoic acid, 3-Thiophenoic acid
CAS Number
88-13-1
Purity
≥ 98% (HPLC)
Molecular Formula
C5H4O2S
Molecular Weight
128.15
MDL Number
MFCD00005467
PubChem ID
6918
Melting Point
130-145 ?C
Appearance
White to off-white crystalline 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

Thiophene-3-carboxylic acid is widely utilized in research focused on:

  • Synthetic Organic Chemistry: It serves as a key building block in the synthesis of various organic compounds, enabling the creation of complex molecules for pharmaceuticals and agrochemicals.
  • Pharmaceutical Development: This compound is used in the development of new drugs, particularly those targeting specific biological pathways, enhancing efficacy and reducing side effects.
  • Material Science: It plays a role in the production of conductive polymers and materials, which are essential in electronics and energy storage applications.
  • Biochemical Research: Researchers utilize it to study metabolic pathways and enzyme interactions, providing insights into biological processes and potential therapeutic targets.
  • Environmental Chemistry: Thiophene-3-carboxylic acid is explored for its potential in developing eco-friendly pesticides and herbicides, offering safer alternatives to traditional chemicals.

Citations