Interesting facts
Interesting Facts about Thiophene-3-Carboxylic Acid
Thiophene-3-carboxylic acid is a fascinating compound in the realm of organic chemistry, specifically in the study of heterocyclic compounds. Not only does it exhibit unique chemical properties, but its structure also opens doors to various applications:
- Structural Significance: This compound contains a thiophene ring, a five-membered aromatic heterocycle that includes a sulfur atom. The presence of sulfur contributes to the compound's distinctive reactivity and stability, making it a subject of interest in the development of new materials.
- Biological Relevance: Thiophene and its derivatives, including thiophene-3-carboxylic acid, have been studied for their biological activities. Some derivatives have shown promise as potential pharmaceutical agents, exhibiting anti-inflammatory and antibacterial properties.
- Synthetic Applications: The carboxylic acid functional group in this compound allows for further chemical transformations. It serves as a precursor in the synthesis of more complex molecules, including agrochemicals, dyes, and organic semiconductors.
- Research Potential: Ongoing research on thiophene-3-carboxylic acid includes its use in organic electronics. The compound has potential applications in electronic devices, owing to its unique electronic properties.
- Polymer Chemistry: This compound may also be engaged in the synthesis of thiophene-based polymers, which are known for their superior conductivity and stability. Such materials are attracting attention in the fields of nanotechnology and materials science.
As said by many chemists, "The more you explore organic compounds, the more you unveil their hidden potentials." Thiophene-3-carboxylic acid stands as an excellent example of how a simple modification in structure can lead to a multitude of intriguing possibilities across various scientific disciplines.
Synonyms
Thiophene-3-carboxylic acid
88-13-1
3-Thiophenecarboxylic acid
3-Thenoic acid
3-thiophenezoic acid
3-Thienylcarboxylic acid
3-Carboxythiophene
MFCD00005467
.beta.-Thiophenic acid
EINECS 201-802-5
NSC 66314
UNII-6V3012Q6BE
BRN 0001994
.beta.-Thiophenecarboxylic acid
6V3012Q6BE
NSC-66314
3-THENOIC ACID [MI]
CHEMBL164585
YNVOMSDITJMNET-UHFFFAOYSA-
DTXSID40236745
5-18-06-00199 (Beilstein Handbook Reference)
beta-Thiophenic acid
beta-Thiophenecarboxylic acid
thiophene-3-carboxylicacid
3-thienoic acid
3-THIOPHENE CARBOXYLIC ACID
3-thiophenecarboxylic
Thiophene-3-formic acid
3-thiophencarboxylic acid
thiophen-3-carboxylic acid
Thiophene-3-caboxylic acid
NCIOpen2_000030
BIDD:GT0807
SCHEMBL152166
DTXCID70159236
3-Thiophenecarboxylic acid, 99%
HMS1738H11
ALBB-012106
NSC66314
BDBM50074328
STK373639
AKOS000276783
AC-4905
CS-W004615
HY-W004615
PB18386
PS-5325
BP-20550
SY001582
DB-016025
NS00039243
T1084
EN300-22996
P17867
AI-942/40179216
Q27265560
F2191-0103
Z147647094
3-Thiophenecarboxylic acid; 3-Thenoic acid; beta-Thiophenic acid
TX0
Solubility of Thiophene-3-carboxylic Acid
Thiophene-3-carboxylic acid, with the formula C5H4O2S, showcases an interesting profile in terms of solubility. This compound is known for its intriguing behavior in various solvents:
In summary, the solubility of thiophene-3-carboxylic acid reflects its chemical structure and the presence of polar functional groups that interact favorably with solvents. Understanding these properties is essential for its applications in various chemical processes and formulations.