4-(2-Amino-phenyl)-piperidine-1-carboxylic acid tert-butyl ester, with the CAS number 199105-03-8, is an organic compound characterized by its piperidine ring structure, which is a six-membered ring containing one nitrogen atom. This compound features an amino group attached to a phenyl ring, contributing to its potential biological activity. The tert-butyl ester group enhances its lipophilicity, which can influence its solubility and permeability in biological systems. Typically, compounds of this nature are studied for their pharmacological properties, particularly in the context of drug development, as they may exhibit activity against various biological targets. The presence of both the amino and carboxylic acid functionalities suggests that this compound could participate in hydrogen bonding, which is crucial for interactions with biological macromolecules. Additionally, the tert-butyl ester moiety may provide stability and protection to the carboxylic acid group during synthesis or in biological environments. Overall, this compound's unique structural features make it a subject of interest in medicinal chemistry and related fields.

4-(2-AMINO-PHENYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

199105-03-8: 4-(2-Amino-phenyl)-piperidine-1-carboxylic acid tert-butyl ester, with the CAS number 199105-03-8, is an organic compound characterized by its piperidine ring structure, which is a six-membered ring containing one nitrogen atom. This compound features an amino group attached to a phenyl ring, contributing to its potential biological activity. The tert-butyl ester group enhances its lipophilicity, which can influence its solubility and permeability in biological systems. Typically, compounds of this nature are studied for their pharmacological properties, particularly in the context of drug development, as they may exhibit activity against various biological targets. The presence of both the amino and carboxylic acid functionalities suggests that this compound could participate in hydrogen bonding, which is crucial for interactions with biological macromolecules. Additionally, the tert-butyl ester moiety may provide stability and protection to the carboxylic acid group during synthesis or in biological environments. Overall, this compound's unique structural features make it a subject of interest in medicinal chemistry and related fields.

1-Piperidinecarboxylic acid, 4-(2-aminophenyl)-, 1,1-dimethylethyl ester

tert-Butyl 4-(2-aminophenyl)piperidine-1-carboxylate

CAS 199105-03-8

4-(2-AMINO-PHENYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

1-Piperidinecarboxylic acid, 4-(2-aminophenyl)-, 1,1-dimethylethyl ester

Ref: IN-DA002BWS

tert-Butyl 4-(2-aminophenyl)piperidine-1-carboxylate

Ref: 54-OR321396

tert-Butyl 4-(2-aminophenyl)piperidine-1-carboxylate

Ref: 10-F640223