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CAS 20972-38-7

:

(2E)-4-(4-bromophenyl)-4-oxobut-2-enoic acid

Description:
(2E)-4-(4-bromophenyl)-4-oxobut-2-enoic acid, with the CAS number 20972-38-7, is an organic compound characterized by its unique structural features. It contains a conjugated system with a double bond and a carbonyl group, which contributes to its reactivity and potential applications in organic synthesis. The presence of the 4-bromophenyl group enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. This compound is likely to exhibit acidic properties due to the carboxylic acid functional group, which can donate protons in solution. Additionally, the geometric configuration indicated by the "(2E)" notation suggests a specific arrangement of substituents around the double bond, influencing its physical and chemical properties. The compound may also display interesting biological activities, making it a candidate for further research in medicinal chemistry. Overall, its structural characteristics suggest potential utility in synthetic organic chemistry and pharmaceuticals.
Formula:C10H7BrO3
InChI:InChI=1/C10H7BrO3/c11-8-3-1-7(2-4-8)9(12)5-6-10(13)14/h1-6H,(H,13,14)/b6-5+
InChI key:InChIKey=CJNVLFPUEBQQMZ-AATRIKPKSA-N
SMILES:C(/C=C/C(O)=O)(=O)C1=CC=C(Br)C=C1
Synonyms:
  • (2E)-4-(4-Bromophenyl)-4-oxo-2-butenoic acid
  • 2-Butenoic acid, 4-(4-bromophenyl)-4-oxo-, (2E)-
  • 2-Butenoic acid, 4-(4-bromophenyl)-4-oxo-, (E)-
  • 3-(4-Bromobenzoyl)acrylic acid
  • Acrylic acid, 3-(p-bromobenzoyl)-, (E)-
  • NSC 39971
  • trans-3-(4-Bromobenzoyl)acrylic acid
  • (2E)-4-(4-Bromophenyl)-4-oxobut-2-enoic acid
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