(S)-3-(4-Chloro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The presence of a 4-chlorophenyl group indicates that there is a chlorine substituent on the phenyl ring, which can influence the compound's biological activity and lipophilicity. The tert-butyl ester functional group suggests that the compound is likely to be more hydrophobic, which can affect its solubility and permeability in biological systems. This compound may exhibit pharmacological properties, potentially acting as a ligand for various receptors or enzymes due to the piperazine structure, which is commonly found in many pharmaceuticals. Its stereochemistry, indicated by the (S) designation, may also play a crucial role in its biological interactions, as different enantiomers can have significantly different effects. Overall, this compound's unique structural features make it of interest in medicinal chemistry and drug development.

(S)-3-(4-CHLORO-PHENYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

1228561-86-1: (S)-3-(4-Chloro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The presence of a 4-chlorophenyl group indicates that there is a chlorine substituent on the phenyl ring, which can influence the compound's biological activity and lipophilicity. The tert-butyl ester functional group suggests that the compound is likely to be more hydrophobic, which can affect its solubility and permeability in biological systems. This compound may exhibit pharmacological properties, potentially acting as a ligand for various receptors or enzymes due to the piperazine structure, which is commonly found in many pharmaceuticals. Its stereochemistry, indicated by the (S) designation, may also play a crucial role in its biological interactions, as different enantiomers can have significantly different effects. Overall, this compound's unique structural features make it of interest in medicinal chemistry and drug development.

(S)-3-(4-Chloro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester

tert-Butyl (S)-3-(4-chlorophenyl)piperazine-1-carboxylate

CAS 1228561-86-1

(S)-3-(4-CHLORO-PHENYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

(S)-3-(4-Chloro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester

Ref: IN-DA01E66W

tert-Butyl (S)-3-(4-chlorophenyl)piperazine-1-carboxylate

Ref: 54-OR88277

tert-Butyl (S)-3-(4-chlorophenyl)piperazine-1-carboxylate

Ref: 10-F616079