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Catalog Number:
17669
CAS Number:
339009-58-4
3-[(4-Chlorobenzyl)oxy]-2-thiophene-carboxylic acid
Purity:
≥ 99%
Synonym(s):
3-[(4-Chlorobenzyl)oxy]-2-thiophenecarboxylic acid
Documents
$89.13 /250MG
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Product Information

3-(4-Chloro-benzyloxy)-thiophene-2-carboxylic acid is a versatile compound with significant applications in the fields of organic synthesis and pharmaceutical development. This compound features a unique thiophene ring structure, which is known for its electronic properties, making it an excellent candidate for use in the development of organic semiconductors and materials for electronic devices. Its chlorobenzyl ether functionality enhances its reactivity, allowing for various substitution reactions that can be utilized in the synthesis of more complex molecules.

In the pharmaceutical industry, this compound can serve as a building block for the synthesis of bioactive molecules, particularly in the development of anti-inflammatory and antimicrobial agents. Researchers have found that the presence of the thiophene moiety can contribute to improved biological activity, making it a valuable addition to medicinal chemistry libraries. Its unique properties and functional groups position it as a promising candidate for further exploration in drug discovery and material science applications.

Synonyms
3-[(4-Chlorobenzyl)oxy]-2-thiophenecarboxylic acid
CAS Number
339009-58-4
Purity
≥ 99%
Molecular Formula
C12H9ClO3S
Molecular Weight
268.72
MDL Number
MFCD00173490
PubChem ID
2764232
Melting Point
156-161 °C
Appearance
Cream solid
Conditions
Store at 0-8°C
General Information
Synonyms
3-[(4-Chlorobenzyl)oxy]-2-thiophenecarboxylic acid
CAS Number
339009-58-4
Purity
≥ 99%
Molecular Formula
C12H9ClO3S
Molecular Weight
268.72
MDL Number
MFCD00173490
PubChem ID
2764232
Melting Point
156-161 °C
Appearance
Cream 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

3-(4-Chloro-benzyloxy)-thiophene-2-carboxylic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and anti-cancer drugs, enhancing therapeutic efficacy.
  • Organic Electronics: It is used in the fabrication of organic semiconductors, contributing to advancements in flexible electronics and organic light-emitting diodes (OLEDs), which are crucial for modern display technologies.
  • Agricultural Chemicals: The compound is explored for its potential as a pesticide or herbicide, providing an eco-friendly alternative to traditional chemicals, thus supporting sustainable agriculture practices.
  • Material Science: It acts as a building block for creating novel materials with unique properties, such as conductive polymers, which can be applied in various industrial applications, including sensors and batteries.
  • Research in Chemical Biology: This compound is utilized in studies examining biological pathways, offering insights into cellular processes and potential therapeutic targets, making it valuable for academic and clinical research.

Citations