Ethyl 3-((4-ethoxyphenyl)amino)-2-((4-methylphenyl)sulfonyl)prop-2-enoate, with the CAS number 1024742-76-4, is an organic compound characterized by its complex structure, which includes an ethyl ester functional group, an amino group, and a sulfonyl moiety. This compound features a prop-2-enoate backbone, indicating it has an unsaturated carbon-carbon double bond, which contributes to its reactivity. The presence of the ethoxy and methylphenyl groups enhances its lipophilicity, potentially influencing its solubility and biological activity. The sulfonyl group is known for its ability to participate in various chemical reactions, making this compound of interest in medicinal chemistry and drug development. Additionally, the compound's structural features suggest potential applications in areas such as pharmaceuticals, where modifications to the aromatic rings can lead to variations in biological activity. Overall, the unique combination of functional groups and structural elements makes this compound a subject of interest for further research and application in various chemical contexts.

ETHYL 3-((4-ETHOXYPHENYL)AMINO)-2-((4-METHYLPHENYL)SULFONYL)PROP-2-ENOATE

1024742-76-4: Ethyl 3-((4-ethoxyphenyl)amino)-2-((4-methylphenyl)sulfonyl)prop-2-enoate, with the CAS number 1024742-76-4, is an organic compound characterized by its complex structure, which includes an ethyl ester functional group, an amino group, and a sulfonyl moiety. This compound features a prop-2-enoate backbone, indicating it has an unsaturated carbon-carbon double bond, which contributes to its reactivity. The presence of the ethoxy and methylphenyl groups enhances its lipophilicity, potentially influencing its solubility and biological activity. The sulfonyl group is known for its ability to participate in various chemical reactions, making this compound of interest in medicinal chemistry and drug development. Additionally, the compound's structural features suggest potential applications in areas such as pharmaceuticals, where modifications to the aromatic rings can lead to variations in biological activity. Overall, the unique combination of functional groups and structural elements makes this compound a subject of interest for further research and application in various chemical contexts.

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CAS 1024742-76-4

ETHYL 3-((4-ETHOXYPHENYL)AMINO)-2-((4-METHYLPHENYL)SULFONYL)PROP-2-ENOATE

ethyl 3-((4-ethoxyphenyl)amino)-2-((4-methylphenyl)sulfonyl)prop-2-enoate

Ref: 3D-ZQB74276