CAS 19418-11-2
:2-Thiophenecarboxylic acid, tetrahydro-
Description:
2-Thiophenecarboxylic acid, tetrahydro- is an organic compound characterized by the presence of a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group (-COOH) attached to the thiophene ring, contributing to its acidic properties. The "tetrahydro" designation indicates that the compound has undergone hydrogenation, resulting in a saturated form of the thiophene ring, which enhances its stability and alters its reactivity compared to its unsaturated counterparts. Typically, compounds like this exhibit moderate solubility in polar solvents due to the presence of the carboxylic acid group, while the thiophene moiety can engage in various chemical reactions, including electrophilic substitutions. The compound may find applications in organic synthesis, pharmaceuticals, and materials science due to its unique structural features and functional properties. As with many organic acids, it may exhibit typical acid-base behavior, participating in proton transfer reactions in solution.
Formula:C5H8O2S
Synonyms:- tetrahydrothiophene-2-carboxylic acid
- 2-Thiophenecarboxylic acid, tetrahydro-
- Tetrahydro-2-thiophenecarboxylic acid
- (2R,5S)-5-(4-Amino-5-Fluoro-2-Oxo-2H-Pyrimidin-Yl)-(1,3)-Oxa - Thiolane-2-Carboxylic Acid,2S-Isopropyl-5R-Methyl-1R-Cyclo
- 2-Thiophenecarboxylic acid, tetrahydro- ISO 9001:2015 REACH
- thiolane-2-carboxylic acid
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Found 4 products.
2-Thiophenecarboxylic acid, tetrahydro-
CAS:Formula:C5H8O2SPurity:98%Color and Shape:SolidMolecular weight:132.1808Thiolane-2-carboxylic acid
CAS:<p>Thiolane-2-carboxylic acid</p>Purity:98%Molecular weight:132.18g/moltetrahydro-2-thiophenecarboxylic acid
CAS:Formula:C5H8O2SPurity:98%Color and Shape:No data available.Molecular weight:132.18Tetrahydrothiophene-2-carboxylic acid
CAS:<p>Tetrahydrothiophene-2-carboxylic acid is a metabolite of tetrahydrothiophene-2-acetic acid. It has been found to be a demethylation product of the protein genes in testicular tissues. Tetrahydrothiophene-2-carboxylic acid has been shown to inhibit the production of human telomerase and consequently, cell proliferation. This compound also inhibits the growth factor activity of bovine erythropoietin, which may be due to its chloride anion. The optical imaging technique has been used to study the effect of tetrahydrothiophene-2-carboxylic acid on cultured cells, revealing that this metabolite may induce apoptosis by increasing oxidative stress and inhibiting the synthesis of proteins essential for cell division.</p>Formula:C5H8O2SPurity:Min. 95%Molecular weight:132.2 g/mol



