Ethyl 2-[(3-chlorophenyl)methyl]-3-methylamino-propanoate, identified by its CAS number 886366-08-1, is an organic compound characterized by its ester functional group, which is typical of ethyl esters. This compound features a propanoate backbone, with a 3-methylamino group that introduces basic properties, potentially influencing its solubility and reactivity. The presence of a 3-chlorophenyl group adds to its complexity, contributing to its aromatic characteristics and potentially affecting its biological activity. The chlorinated aromatic ring can enhance lipophilicity, which may influence the compound's pharmacokinetics if it is biologically active. Ethyl esters are generally known for their pleasant odors and are often used in flavoring and fragrance applications. Additionally, the specific arrangement of substituents in this compound suggests potential interactions in biological systems, making it of interest in medicinal chemistry. Overall, this compound's unique structure may lead to diverse applications, particularly in pharmaceuticals or agrochemicals, depending on its biological properties and reactivity.

ethyl 2-[(3-chlorophenyl)methyl]-3-methylamino-propanoate

886366-08-1: Ethyl 2-[(3-chlorophenyl)methyl]-3-methylamino-propanoate, identified by its CAS number 886366-08-1, is an organic compound characterized by its ester functional group, which is typical of ethyl esters. This compound features a propanoate backbone, with a 3-methylamino group that introduces basic properties, potentially influencing its solubility and reactivity. The presence of a 3-chlorophenyl group adds to its complexity, contributing to its aromatic characteristics and potentially affecting its biological activity. The chlorinated aromatic ring can enhance lipophilicity, which may influence the compound's pharmacokinetics if it is biologically active. Ethyl esters are generally known for their pleasant odors and are often used in flavoring and fragrance applications. Additionally, the specific arrangement of substituents in this compound suggests potential interactions in biological systems, making it of interest in medicinal chemistry. Overall, this compound's unique structure may lead to diverse applications, particularly in pharmaceuticals or agrochemicals, depending on its biological properties and reactivity.

CAS 886366-08-1

ethyl 2-[(3-chlorophenyl)methyl]-3-methylamino-propanoate

ETHYL 3-(3-CHLORO-PHENYL)-2-METHYLAMINOMETHYL-PROPIONATE

Ref: IN-DA0049LE