The chemical substance known as "2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(3-hydroxyphenyl)-, (E)-" with CAS number 88191-18-8 is an organic compound characterized by its structure, which includes a conjugated system featuring an α,β-unsaturated carbonyl group. This compound exhibits properties typical of phenolic compounds, including potential antioxidant activity due to the presence of multiple hydroxyl groups on the aromatic rings. The (E)-configuration indicates that the substituents around the double bond are in a trans arrangement, which can influence its reactivity and interactions with biological systems. The presence of hydroxyl groups enhances its solubility in polar solvents and may contribute to its biological activity. Additionally, this compound may be studied for its potential applications in pharmaceuticals, particularly in the context of its effects on oxidative stress and related pathways. Overall, its unique structural features and functional groups make it a subject of interest in both synthetic and medicinal chemistry.

2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(3-hydroxyphenyl)-, (E)-

88191-18-8: The chemical substance known as "2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(3-hydroxyphenyl)-, (E)-" with CAS number 88191-18-8 is an organic compound characterized by its structure, which includes a conjugated system featuring an α,β-unsaturated carbonyl group. This compound exhibits properties typical of phenolic compounds, including potential antioxidant activity due to the presence of multiple hydroxyl groups on the aromatic rings. The (E)-configuration indicates that the substituents around the double bond are in a trans arrangement, which can influence its reactivity and interactions with biological systems. The presence of hydroxyl groups enhances its solubility in polar solvents and may contribute to its biological activity. Additionally, this compound may be studied for its potential applications in pharmaceuticals, particularly in the context of its effects on oxidative stress and related pathways. Overall, its unique structural features and functional groups make it a subject of interest in both synthetic and medicinal chemistry.

CAS 88191-18-8

2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(3-hydroxyphenyl)-, (E)-

2-Propen-1-one, 3-(3,4-dihydroxyphenyl)-1-(3-hydroxyphenyl)-, (E)-

Ref: IN-DA004C9Y