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CAS 898282-25-2

:

(S)-1-Boc-4-benzylpiperazine-2-carboxylic acid

Description:
(S)-1-Boc-4-benzylpiperazine-2-carboxylic acid is a chiral 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 facilitating its use in various synthetic applications. The presence of the benzyl group contributes to the compound's lipophilicity, potentially influencing its biological activity and solubility. The carboxylic acid functional group is crucial for its reactivity and can participate in various chemical reactions, such as esterification or amidation. This compound is often utilized in medicinal chemistry and drug development due to its structural features that may interact with biological targets. Its chirality, indicated by the "(S)" designation, suggests that it may exhibit specific pharmacological properties, making it of interest in the design of enantiomerically pure drugs. Overall, (S)-1-Boc-4-benzylpiperazine-2-carboxylic acid is a versatile building block in organic synthesis and pharmaceutical research.
Formula:C17H24N2O4
InChI:InChI=1/C17H24N2O4/c1-17(2,3)23-16(22)19-10-9-18(12-14(19)15(20)21)11-13-7-5-4-6-8-13/h4-8,14H,9-12H2,1-3H3,(H,20,21)/t14-/m0/s1
SMILES:CC(C)(C)OC(=O)N1CCN(Cc2ccccc2)C[C@H]1C(=O)O
Synonyms:
  • 1,2-piperazinedicarboxylic acid, 4-(phenylmethyl)-, 1-(1,1-dimethylethyl) ester, (2S)-
  • (2S)-4-benzyl-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
  • (S)-4-benzyl-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
  • (S)-1-Boc-4-benzylpiperazine-2-carboxylic acid
  • 4-BENZYL-PIPERAZINE-1,2-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER HYDROCHLORIDE
  • ZGEORLKSWXAMBW-AWEZNQCLSA-N
  • (2S)-4-benzyl-1-[(2-methylpropan-2-yl)oxycarbonyl]piperazine-2-carboxylic acid
  • 4-Benzyl-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid hydrochloride
  • (S)-1-(tert-butoxycarbonyl)-4-benzylpiperazine-2-carboxylic acid
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