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CAS 13565-07-6

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(2E)-3-(4-Methylphenyl)-2-propenoyl chloride

Description:
(2E)-3-(4-Methylphenyl)-2-propenoyl chloride, with the CAS number 13565-07-6, is an organic compound characterized by its functional groups and structural features. It contains a propenoyl moiety, which is a vinyl group attached to a carbonyl, indicating its potential reactivity in various chemical reactions, particularly in acylation and polymerization processes. The presence of the 4-methylphenyl group suggests that it has aromatic characteristics, contributing to its stability and influencing its reactivity. As an acyl chloride, it is expected to be a reactive compound, particularly with nucleophiles, and can readily undergo hydrolysis to form the corresponding acid. This compound is typically used in organic synthesis, particularly in the preparation of more complex molecules. Its physical properties, such as boiling point and solubility, would be influenced by the presence of the aromatic ring and the acyl chloride functional group. Safety precautions should be taken when handling this compound, as acyl chlorides can be corrosive and may release harmful gases upon reaction with water.
Formula:C10H9ClO
InChI:InChI=1S/C10H9ClO/c1-8-2-4-9(5-3-8)6-7-10(11)12/h2-7H,1H3/b7-6+
InChI key:InChIKey=ARGVABDJPRRAQI-VOTSOKGWSA-N
SMILES:C(=C/C(Cl)=O)\C1=CC=C(C)C=C1
Synonyms:
  • (E)-p-Methylcinnamoyl chloride
  • (2E)-3-(4-Methylphenyl)-2-propenoyl chloride
  • 2-Propenoyl chloride, 3-(4-methylphenyl)-, (2E)-
  • 2-Propenoyl chloride, 3-(4-methylphenyl)-, (E)-
  • Cinnamoyl chloride, p-methyl-, (E)-
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