The chemical substance known as (2E)-3-(6-chloro-4-oxo-4H-chromen-3-yl)prop-2-enoic acid, with the CAS number 42059-70-1, is a synthetic organic compound that belongs to the class of chromenone derivatives. This compound features a chromenone moiety, characterized by a fused benzene and pyrone ring, which contributes to its potential biological activity. The presence of a chloro substituent at the 6-position enhances its reactivity and may influence its pharmacological properties. The prop-2-enoic acid functional group indicates that it possesses an α,β-unsaturated carboxylic acid structure, which is known for its ability to participate in various chemical reactions, including Michael additions and condensation reactions. This compound may exhibit interesting properties such as antioxidant, anti-inflammatory, or anticancer activities, making it a subject of interest in medicinal chemistry and drug development. Its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups in a given formulation.

(2E)-3-(6-chloro-4-oxo-4H-chromen-3-yl)prop-2-enoic acid

42059-70-1: The chemical substance known as (2E)-3-(6-chloro-4-oxo-4H-chromen-3-yl)prop-2-enoic acid, with the CAS number 42059-70-1, is a synthetic organic compound that belongs to the class of chromenone derivatives. This compound features a chromenone moiety, characterized by a fused benzene and pyrone ring, which contributes to its potential biological activity. The presence of a chloro substituent at the 6-position enhances its reactivity and may influence its pharmacological properties. The prop-2-enoic acid functional group indicates that it possesses an α,β-unsaturated carboxylic acid structure, which is known for its ability to participate in various chemical reactions, including Michael additions and condensation reactions. This compound may exhibit interesting properties such as antioxidant, anti-inflammatory, or anticancer activities, making it a subject of interest in medicinal chemistry and drug development. Its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups in a given formulation.

CAS 42059-70-1

(2E)-3-(6-chloro-4-oxo-4H-chromen-3-yl)prop-2-enoic acid

(2E)-3-(6-chloro-4-oxo-4H-chromen-3-yl)acrylic acid

Ref: 10-F314991