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CAS 189331-48-4

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Ethyl 5-(difluoromethyl)-3-thiophenecarboxylate

Description:
Ethyl 5-(difluoromethyl)-3-thiophenecarboxylate is an organic compound characterized by its unique structure, which includes a thiophene ring and a difluoromethyl group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its potential applications in medicinal chemistry and as an intermediate in the synthesis of various pharmaceuticals. The presence of the difluoromethyl group enhances its biological activity and lipophilicity, making it a subject of interest in drug development. Ethyl 5-(difluoromethyl)-3-thiophenecarboxylate is generally stable under standard conditions but may undergo hydrolysis or other reactions under specific circumstances. It is important to handle this compound with care, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken during its use in laboratory settings. As with many organic compounds, its reactivity can be influenced by the presence of functional groups and the overall molecular environment.
Formula:C8H8F2O2S
InChI:InChI=1S/C8H8F2O2S/c1-2-12-8(11)5-3-6(7(9)10)13-4-5/h3-4,7H,2H2,1H3
InChI key:InChIKey=ZHHJKCZFRWRCPG-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C=C(C(F)F)SC1
Synonyms:
  • Ethyl 5-(difluoromethyl)-3-thiophenecarboxylate
  • 3-Thiophenecarboxylic acid, 5-(difluoromethyl)-, ethyl ester
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