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CAS 6552-63-2

:

1-(4-Chlorophenyl)-3-(4-methoxyphenyl)-2-propen-1-one

Description:
1-(4-Chlorophenyl)-3-(4-methoxyphenyl)-2-propen-1-one, commonly referred to as a chalcone, is an organic compound characterized by its conjugated double bond system, which contributes to its reactivity and potential biological activity. This compound features a central α,β-unsaturated carbonyl group flanked by two aromatic rings: one containing a chlorine substituent and the other a methoxy group. The presence of these substituents can influence the compound's electronic properties, solubility, and overall reactivity. Chalcones are known for their diverse biological activities, including anti-inflammatory, antioxidant, and anticancer properties, making them of interest in medicinal chemistry. The compound's structure allows for potential interactions with various biological targets, and its synthesis typically involves the Claisen-Schmidt condensation reaction. Additionally, its stability and reactivity can be affected by environmental factors such as pH and temperature, which are important considerations in both laboratory and industrial applications. Overall, this compound exemplifies the rich chemistry associated with chalcones and their derivatives.
Formula:C16H13ClO2
InChI:InChI=1S/C16H13ClO2/c1-19-15-9-2-12(3-10-15)4-11-16(18)13-5-7-14(17)8-6-13/h2-11H,1H3
InChI key:InChIKey=KGKFNDADSPFRCJ-UHFFFAOYSA-N
SMILES:C(C=CC1=CC=C(OC)C=C1)(=O)C2=CC=C(Cl)C=C2
Synonyms:
  • (2E)-1-(4-Chlorophenyl)-3-(4-methoxyphenyl)-2-propen-1-one
  • 1-(4-Chlorophenyl)-3-(4-methoxyphenyl)-2-propen-1-one
  • 2-Propen-1-one, 1-(4-chlorophenyl)-3-(4-methoxyphenyl)-
  • 2-Propen-1-one, 1-(4-chlorophenyl)-3-(4-methoxyphenyl)-, (2E)-
  • 4′-Chloro-4-methoxychalcone
  • 6552-63-2
  • Chalcone, 4′-chloro-4-methoxy-
  • NSC 83482
  • trans-4'-Chloro-4-methoxychalcone
  • (2E)-1-(4-Chlorophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one
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