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CAS 39856-08-1

:

(2E)-3-(3,4-dimethoxyphenyl)prop-2-enoyl chloride

Description:
(2E)-3-(3,4-dimethoxyphenyl)prop-2-enoyl chloride, with the CAS number 39856-08-1, is an organic compound characterized by its enoyl chloride functional group, which is known for its reactivity in acylation reactions. This compound features a prop-2-enoyl moiety, indicating the presence of a double bond between the second and third carbon atoms, contributing to its unsaturation and potential for further chemical transformations. The presence of the 3,4-dimethoxyphenyl group suggests that it has significant aromatic characteristics, which can influence its reactivity and solubility. The methoxy groups enhance the electron density of the aromatic ring, potentially affecting its electrophilic substitution reactions. As an acyl chloride, it is likely to be a potent acylating agent, making it useful in organic synthesis, particularly in the formation of esters and amides. Additionally, due to the presence of the acyl chloride functional group, it may be sensitive to moisture and should be handled with care to avoid hydrolysis.
Formula:C11H11ClO3
InChI:InChI=1/C11H11ClO3/c1-14-9-5-3-8(4-6-11(12)13)7-10(9)15-2/h3-7H,1-2H3/b6-4+
Synonyms:
  • (2E)-3-(3,4-Dimethoxyphenyl)acryloyl chloride
  • 2-propenoyl chloride, 3-(3,4-dimethoxyphenyl)-, (2E)-
  • 3,4-Dimethoxycinnamoyl chloride
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