The chemical substance known as 2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, (2E)-3-phenyl-2-propenyl ester, (2E)-, with CAS number 115610-31-6, is an organic compound characterized by its ester functional group and a propenoic acid backbone. This compound features a phenyl group and a substituted phenolic moiety, which contributes to its potential biological activity and reactivity. The presence of the methoxy and hydroxy groups on the aromatic ring enhances its solubility in organic solvents and may influence its interaction with biological systems. The (2E) configuration indicates that the double bond in the propenyl chain has a specific geometric arrangement, which can affect the compound's reactivity and stability. This substance may be of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in drug development or as a precursor in polymer synthesis. Its unique structural features suggest that it could exhibit interesting chemical properties, including reactivity in polymerization reactions or interactions with biological targets.

2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-,(2E)-3-phenyl-2-propenyl ester, (2E)-

115610-31-6: The chemical substance known as 2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, (2E)-3-phenyl-2-propenyl ester, (2E)-, with CAS number 115610-31-6, is an organic compound characterized by its ester functional group and a propenoic acid backbone. This compound features a phenyl group and a substituted phenolic moiety, which contributes to its potential biological activity and reactivity. The presence of the methoxy and hydroxy groups on the aromatic ring enhances its solubility in organic solvents and may influence its interaction with biological systems. The (2E) configuration indicates that the double bond in the propenyl chain has a specific geometric arrangement, which can affect the compound's reactivity and stability. This substance may be of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in drug development or as a precursor in polymer synthesis. Its unique structural features suggest that it could exhibit interesting chemical properties, including reactivity in polymerization reactions or interactions with biological targets.

<p>Cinnamyl isoferulate is a natural product of Populus, Salicaceae.</p>

CAS 115610-31-6

2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-,(2E)-3-phenyl-2-propenyl ester, (2E)-

Cinnamyl isoferulate

Ref: TM-TN3662

Ferulic Acid Impurity 12

Ref: 4Z-F-155013