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Atomfair Methyl 3-(thiophen-2-yl)propanoate C8H10O2S

Description Methyl 3-(thiophen-2-yl)propanoate (CAS No. 1693-86-3) is a high-purity organic compound with the molecular formula C8H10O2S . This ester derivative of thiophene is a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name, methyl 3-thiophen-2-ylpropanoate , reflects its structural composition, featuring a thiophene ring linked to a propanoate ester group. Available in various quantities, this compound is rigorously tested for quality, ensuring optimal performance in research applications. Suitable for use in analytical standards, chemical synthesis, and material science, it is packaged under controlled conditions to maintain stability and purity.

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Description

Description

Methyl 3-(thiophen-2-yl)propanoate (CAS No. 1693-86-3) is a high-purity organic compound with the molecular formula C8H10O2S. This ester derivative of thiophene is a valuable intermediate in organic synthesis and pharmaceutical research. Its IUPAC name, methyl 3-thiophen-2-ylpropanoate, reflects its structural composition, featuring a thiophene ring linked to a propanoate ester group. Available in various quantities, this compound is rigorously tested for quality, ensuring optimal performance in research applications. Suitable for use in analytical standards, chemical synthesis, and material science, it is packaged under controlled conditions to maintain stability and purity.

  • CAS No: 1693-86-3
  • Molecular Formula: C8H10O2S
  • Molecular Weight: 170.23
  • Exact Mass: 170.04015073
  • Monoisotopic Mass: 170.04015073
  • IUPAC Name: methyl 3-thiophen-2-ylpropanoate
  • SMILES: COC(=O)CCC1=CC=CS1
  • Synonyms: 16862-05-8, Methyl 3-(thiophen-2-yl)propanoate, DTXSID90340664, DTXCID10291745, 964-554-3

Application

Methyl 3-(thiophen-2-yl)propanoate is widely utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials. Its thiophene moiety makes it a valuable precursor for heterocyclic compounds with potential biological activity. Researchers employ this ester in coupling reactions, polymer chemistry, and as a building block for complex organic frameworks. It is also investigated for its role in developing novel materials with optoelectronic properties.

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