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CAS 10263-19-1

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3′,4′,5′-Trimethoxycinnamoyl chloride

Description:
3′,4′,5′-Trimethoxycinnamoyl chloride is an organic compound characterized by its structure, which includes a cinnamoyl moiety substituted with three methoxy groups at the 3′, 4′, and 5′ positions of the aromatic ring, along with a reactive acyl chloride functional group. This compound typically appears as a solid or crystalline substance and is known for its reactivity, particularly due to the presence of the acyl chloride group, which can readily undergo nucleophilic substitution reactions. It is often utilized in organic synthesis, particularly in the preparation of various derivatives and in the development of pharmaceuticals and agrochemicals. The methoxy groups enhance its solubility in organic solvents and may influence its biological activity. As with many acyl chlorides, it is important to handle this compound with care, as it can be corrosive and may release hydrochloric acid upon reaction with water or moisture. Proper safety precautions should be taken when working with this substance in a laboratory setting.
Formula:C12H13ClO4
InChI:InChI=1S/C12H13ClO4/c1-15-9-6-8(4-5-11(13)14)7-10(16-2)12(9)17-3/h4-7H,1-3H3
InChI key:InChIKey=NFFPFTGFVSWSTH-UHFFFAOYSA-N
SMILES:O(C)C1=C(OC)C(OC)=CC(C=CC(Cl)=O)=C1
Synonyms:
  • (2E)-3-(3,4,5-Trimethoxyphenyl)acryloyl chloride
  • 2-Propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-
  • 2-propenoyl chloride, 3-(3,4,5-trimethoxyphenyl)-, (2E)-
  • 3,4,5-Trimethoxycinnamoyl chloride
  • 3-(3,4,5-Trimethoxyphenyl)-2-propenoyl chloride
  • Cinnamoyl chloride, 3,4,5-trimethoxy-
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