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CAS 22966-09-2

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(2E)-3-(4-bromophenyl)-1-phenylprop-2-en-1-one

Description:
The chemical substance known as (2E)-3-(4-bromophenyl)-1-phenylprop-2-en-1-one, with the CAS number 22966-09-2, is an organic compound characterized by its conjugated double bond system and the presence of a bromine atom on the phenyl ring. This compound features a chalcone structure, which is typically known for its role in various biological activities, including anti-inflammatory and antioxidant properties. The presence of the bromine substituent enhances its reactivity and may influence its biological interactions. The compound is likely to exhibit a yellow to orange color, typical of many chalcones, and is soluble in organic solvents. Its molecular structure allows for potential applications in organic synthesis and as a precursor in the development of pharmaceuticals. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the bromine atom and the phenyl groups, making it a subject of interest in both synthetic and medicinal chemistry.
Formula:C15H11BrO
InChI:InChI=1/C15H11BrO/c16-14-9-6-12(7-10-14)8-11-15(17)13-4-2-1-3-5-13/h1-11H/b11-8+
Synonyms:
  • (2E)-3-(4-Bromophenyl)-1-phenyl-2-propen-1-one
  • 2-Propen-1-one, 3- (4-bromophenyl)-1-phenyl-
  • 2-propen-1-one, 3-(4-bromophenyl)-1-phenyl-, (2E)-
  • 2-Propen-1-one, 3-(4-bromophenyl)-1-phenyl-, (E)-
  • trans-4-Bromochalcone
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