Diethyl [(4-chlorophenyl)amino]propanedioate, with the CAS number 5203-01-0, is an organic compound characterized by its ester functional groups and an amine moiety. It features a diethyl ester of a propanedioic acid derivative, where one of the hydrogen atoms in the amine group is substituted by a 4-chlorophenyl group. This substitution imparts specific chemical properties, including potential biological activity, making it of interest in medicinal chemistry. The presence of the chlorophenyl group can enhance lipophilicity, affecting the compound's solubility and permeability in biological systems. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It may exhibit moderate to high stability under standard conditions but should be handled with care due to potential toxicity associated with the chlorinated aromatic ring. As with many organic compounds, it is important to consider its reactivity, potential for hydrolysis, and interactions with other chemical species in various environments.

diethyl [(4-chlorophenyl)amino]propanedioate

5203-01-0: Diethyl [(4-chlorophenyl)amino]propanedioate, with the CAS number 5203-01-0, is an organic compound characterized by its ester functional groups and an amine moiety. It features a diethyl ester of a propanedioic acid derivative, where one of the hydrogen atoms in the amine group is substituted by a 4-chlorophenyl group. This substitution imparts specific chemical properties, including potential biological activity, making it of interest in medicinal chemistry. The presence of the chlorophenyl group can enhance lipophilicity, affecting the compound's solubility and permeability in biological systems. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and temperature. It may exhibit moderate to high stability under standard conditions but should be handled with care due to potential toxicity associated with the chlorinated aromatic ring. As with many organic compounds, it is important to consider its reactivity, potential for hydrolysis, and interactions with other chemical species in various environments.

<p>Diethyl 2-(4-chlorophenylamino)malonate</p>

CAS 5203-01-0

diethyl [(4-chlorophenyl)amino]propanedioate

Diethyl 2-(4-chlorophenylamino)malonate

Ref: 54-OR300729