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CAS 6028-89-3

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1-(4-Methylphenyl)-3-(2-thienyl)-2-propen-1-one

Description:
1-(4-Methylphenyl)-3-(2-thienyl)-2-propen-1-one, also known as a type of chalcone, is an organic compound characterized by its distinctive structure, which includes a chalcone backbone featuring a 4-methylphenyl group and a thienyl group. This compound typically appears as a yellow to orange crystalline solid and is known for its potential biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. The presence of the thienyl ring contributes to its unique electronic properties, which can influence its reactivity and interaction with other molecules. Chalcones like this one are often studied for their role in organic synthesis and as intermediates in the production of various pharmaceuticals and agrochemicals. Additionally, they may exhibit interesting photophysical properties, making them candidates for applications in materials science and organic electronics. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity or reactivity.
Formula:C14H12OS
InChI:InChI=1/C14H12OS/c1-11-4-6-12(7-5-11)14(15)9-8-13-3-2-10-16-13/h2-10H,1H3/b9-8+
InChI key:InChIKey=OUDDTWPBSXBJOY-UHFFFAOYSA-N
SMILES:C(C=CC1=CC=CS1)(=O)C2=CC=C(C)C=C2
Synonyms:
  • (2E)-1-(4-methylphenyl)-3-(thiophen-2-yl)prop-2-en-1-one
  • 1-(4-Methylphenyl)-3-(2-thienyl)-2-propen-1-one
  • 1-(4-Methylphenyl)-3-(Thiophen-2-Yl)Prop-2-En-1-One
  • 1-(4-Methylphenyl)-3-(thien-2-yl)-2-propen-1-one
  • 2-Propen-1-one, 1-(4-methylphenyl)-3-(2-thienyl)-
  • 3-(2-Thienyl)-1-(p-tolyl)-prop-2-en-1-one
  • Acrylophenone, 4′-methyl-3-(2-thienyl)-
  • 1-(4-METHYLPHENYL)-3-(THIEN-2-YL)PROP-2-EN-1-ONE
  • (2E)-1-(4-Methylphenyl)-3-(2-thienyl)-2-propen-1-one
  • 1-(4-METHYLPHENYL)-3-(2-THIENYL)PROP-2-EN-1-ONE
  • 3-(2-THIENYL)-1-(P-TOLYL)-2-PROPEN-1-ONE, 98%
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