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CAS 175136-00-2

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3-(2-Chloro-3,4-dimethoxyphenyl)-2-propenoyl chloride

Description:
3-(2-Chloro-3,4-dimethoxyphenyl)-2-propenoyl chloride, with the CAS number 175136-00-2, is an organic compound characterized by its acyl chloride functional group, which is known for its reactivity in various chemical reactions, particularly in acylation processes. This compound features a propenoyl moiety attached to a chlorinated aromatic ring that is further substituted with two methoxy groups, contributing to its unique chemical properties. The presence of the chlorine atom enhances its electrophilicity, making it a useful intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. The methoxy groups can influence the compound's solubility and reactivity, while the overall structure suggests potential applications in the development of biologically active molecules. As with many acyl chlorides, it is likely to be sensitive to moisture and should be handled with care to avoid hydrolysis, which can lead to the formation of the corresponding carboxylic acid. Proper storage and handling protocols are essential to maintain its stability and reactivity.
Formula:C11H10Cl2O3
InChI:InChI=1S/C11H10Cl2O3/c1-15-8-5-3-7(4-6-9(12)14)10(13)11(8)16-2/h3-6H,1-2H3
InChI key:InChIKey=LUJOUFWJHFXYKV-UHFFFAOYSA-N
SMILES:O(C)C1=C(OC)C=CC(C=CC(Cl)=O)=C1Cl
Synonyms:
  • (2E)-3-(2-chloro-3,4-dimethoxyphenyl)prop-2-enoyl chloride
  • 2-Propenoyl chloride, 3-(2-chloro-3,4-dimethoxyphenyl)-
  • 3-(2-Chloro-3,4-Dimethoxyphenyl)Acryloyl Chloride
  • 3-(2-Chloro-3,4-dimethoxyphenyl)-2-propenoyl chloride
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