Ethyl 1-(3-amino-4-nitrophenyl)-4-piperidinecarboxylate, identified by its CAS number 439095-45-1, is a chemical compound characterized by its complex structure, which includes an ethyl ester group, an amino group, and a nitrophenyl moiety. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents, reflecting its polar and non-polar characteristics due to the presence of both hydrophilic and hydrophobic functional groups. The nitro group contributes to its potential reactivity and biological activity, making it of interest in medicinal chemistry and drug development. The piperidine ring provides a cyclic amine structure that can influence the compound's pharmacological properties, such as its ability to interact with biological targets. Additionally, the presence of the amino group may enhance its solubility and reactivity, making it a versatile intermediate in organic synthesis. Overall, this compound's unique combination of functional groups suggests potential applications in pharmaceuticals, particularly in the development of therapeutic agents.

ETHYL 1-(3-AMINO-4-NITROPHENYL)-4-PIPERIDINECARBOXYLATE

439095-45-1: Ethyl 1-(3-amino-4-nitrophenyl)-4-piperidinecarboxylate, identified by its CAS number 439095-45-1, is a chemical compound characterized by its complex structure, which includes an ethyl ester group, an amino group, and a nitrophenyl moiety. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents, reflecting its polar and non-polar characteristics due to the presence of both hydrophilic and hydrophobic functional groups. The nitro group contributes to its potential reactivity and biological activity, making it of interest in medicinal chemistry and drug development. The piperidine ring provides a cyclic amine structure that can influence the compound's pharmacological properties, such as its ability to interact with biological targets. Additionally, the presence of the amino group may enhance its solubility and reactivity, making it a versatile intermediate in organic synthesis. Overall, this compound's unique combination of functional groups suggests potential applications in pharmaceuticals, particularly in the development of therapeutic agents.

Ethyl 1-(3-amino-4-nitrophenyl)piperidine-4-carboxylate

CAS 439095-45-1

ETHYL 1-(3-AMINO-4-NITROPHENYL)-4-PIPERIDINECARBOXYLATE

Ethyl 1-(3-amino-4-nitrophenyl)piperidine-4-carboxylate

Ref: 54-OR183520