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Atomfair 5-Oxo-5-(2-thienyl)valeric acid C9H10O3S
Description 5-Oxo-5-(2-thienyl)valeric acid (CAS No. 26120-86-5) is a high-purity organic compound with the molecular formula C9H10O3S and IUPAC name 5-oxo-5-thiophen-2-ylpentanoic acid . This specialized chemical features a thiophene moiety linked to a valeric acid backbone, making it a valuable intermediate for pharmaceutical synthesis, material science, and organic research. Our product is rigorously tested to ensure ??98% purity (HPLC/GC), with trace metal analysis confirming suitability for sensitive applications. Supplied as a white to off-white crystalline powder, it is packaged under inert gas to maintain stability. Solubility data (DMSO, ethanol) and detailed spectral profiles (FTIR, NMR, MS) are available upon request. Store…
Description
Description
5-Oxo-5-(2-thienyl)valeric acid (CAS No. 26120-86-5) is a high-purity organic compound with the molecular formula C9H10O3S and IUPAC name 5-oxo-5-thiophen-2-ylpentanoic acid. This specialized chemical features a thiophene moiety linked to a valeric acid backbone, making it a valuable intermediate for pharmaceutical synthesis, material science, and organic research. Our product is rigorously tested to ensure ??98% purity (HPLC/GC), with trace metal analysis confirming suitability for sensitive applications. Supplied as a white to off-white crystalline powder, it is packaged under inert gas to maintain stability. Solubility data (DMSO, ethanol) and detailed spectral profiles (FTIR, NMR, MS) are available upon request. Store at 2-8??C in a tightly sealed container to prevent degradation.
- CAS No: 26120-86-5
- Molecular Formula: C9H10O3S
- Molecular Weight: 198.24
- Exact Mass: 198.03506535
- Monoisotopic Mass: 198.03506535
- IUPAC Name: 5-oxo-5-thiophen-2-ylpentanoic acid
- SMILES: C1=CSC(=C1)C(=O)CCCC(=O)O
- Synonyms: 22971-62-6, 5-Oxo-5-(2-thienyl)valeric acid, 5-Oxo-5-(thiophen-2-yl)pentanoic acid, 4-(2-thienoyl)butyric acid, 5-oxo-5-thiophen-2-ylpentanoic acid
Application
5-Oxo-5-(2-thienyl)valeric acid serves as a key building block in the synthesis of thiophene-containing pharmaceuticals, particularly for CNS-targeting compounds. It is utilized in the development of novel heterocyclic frameworks for material science applications, including conductive polymers. Researchers employ this compound as a precursor for functionalized thiophene derivatives in medicinal chemistry studies.
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