(3S)-4-BOC-1-Carbomethyl-3-isobutyl-piperazin-2-one, identified by its CAS number 959584-21-5, is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The "BOC" (tert-butyloxycarbonyl) group serves as a protective group for the amine, enhancing the compound's stability and solubility in organic solvents. The presence of the isobutyl group contributes to its hydrophobic characteristics, while the carboxymethyl group introduces a polar functional group, which can influence its reactivity and interactions in biological systems. This compound is often utilized in medicinal chemistry and drug development due to its potential biological activity, particularly in the context of designing pharmaceuticals that target specific receptors or enzymes. Its stereochemistry, indicated by the (3S) designation, suggests that it has a specific spatial arrangement that may be crucial for its biological function. Overall, this compound exemplifies the complexity and versatility of piperazine derivatives in chemical synthesis and pharmaceutical applications.

(3S)-4-BOC-1-CARBOXYMETHYL-3-ISOBUTYL-PIPERAZIN-2-ONE

959584-21-5: (3S)-4-BOC-1-Carbomethyl-3-isobutyl-piperazin-2-one, identified by its CAS number 959584-21-5, is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. The "BOC" (tert-butyloxycarbonyl) group serves as a protective group for the amine, enhancing the compound's stability and solubility in organic solvents. The presence of the isobutyl group contributes to its hydrophobic characteristics, while the carboxymethyl group introduces a polar functional group, which can influence its reactivity and interactions in biological systems. This compound is often utilized in medicinal chemistry and drug development due to its potential biological activity, particularly in the context of designing pharmaceuticals that target specific receptors or enzymes. Its stereochemistry, indicated by the (3S) designation, suggests that it has a specific spatial arrangement that may be crucial for its biological function. Overall, this compound exemplifies the complexity and versatility of piperazine derivatives in chemical synthesis and pharmaceutical applications.

CAS 959584-21-5

(3S)-4-BOC-1-CARBOXYMETHYL-3-ISOBUTYL-PIPERAZIN-2-ONE

(3S)-4-Boc-1-carboxymethyl-3-isobutyl-piperazin-2-one

Ref: IN-DA00IJOA