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CAS 14063-77-5

:

3-Chloro-3-(4-chlorophenyl)-2-propenal

Description:
3-Chloro-3-(4-chlorophenyl)-2-propenal, with the CAS number 14063-77-5, is an organic compound characterized by its structure, which includes a propenal moiety with a chlorinated phenyl group. This compound typically appears as a colorless to pale yellow liquid and has a distinct odor. It is known for its reactivity due to the presence of both the aldehyde functional group and the double bond in the propenal structure, making it susceptible to nucleophilic attack. The chlorinated phenyl group enhances its electrophilic character, which can be exploited in various chemical reactions, including nucleophilic addition and substitution reactions. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical and agrochemical research. Its solubility in organic solvents and limited solubility in water are typical for such compounds, and it should be handled with care due to potential toxicity and environmental impact. Proper safety measures should be observed when working with this substance in laboratory settings.
Formula:C9H6Cl2O
InChI:InChI=1S/C9H6Cl2O/c10-8-3-1-7(2-4-8)9(11)5-6-12/h1-6H
InChI key:InChIKey=IWQMAUVMLFGNGU-UHFFFAOYSA-N
SMILES:C(=CC=O)(Cl)C1=CC=C(Cl)C=C1
Synonyms:
  • (2Z)-3-Chloro-3-(4-chlorophenyl)acrylaldehyde
  • 2-Propenal, 3-chloro-3-(4-chlorophenyl)-
  • 2-Propenal, 3-chloro-3-(4-chlorophenyl)-, (2Z)-
  • 3-(4-Chlorophenyl)-3-chloroacrylaldehyde
  • 3-Chloro-3-(4-chlorophenyl)-2-propenal
  • Cinnamaldehyde, p,β-dichloro-
  • p,β-Dichlorocinnamaldehyde
  • α-Chloro-β-formyl-p-chlorostyrene
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