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CAS 167262-68-2

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BOC-4-phenylpiperidine-4-Carboxylic acid

Description:
BOC-4-phenylpiperidine-4-carboxylic acid is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. The "BOC" (tert-butyloxycarbonyl) group is a common protecting group used in organic synthesis, particularly in peptide chemistry, to protect amines. The presence of the phenyl group indicates that there is a phenyl substituent attached to the piperidine ring, contributing to the compound's hydrophobic characteristics. The carboxylic acid functional group (-COOH) provides acidic properties and can participate in various chemical reactions, such as esterification or amidation. This compound is often utilized in pharmaceutical research and development, particularly in the synthesis of potential drug candidates. Its molecular structure allows for interactions with biological targets, making it of interest in medicinal chemistry. As with many organic compounds, proper handling and storage are essential due to potential reactivity and safety considerations.
Formula:C17H22NO4
InChI:InChI=1/C17H23NO4/c1-16(2,3)22-15(21)18-11-9-17(10-12-18,14(19)20)13-7-5-4-6-8-13/h4-8H,9-12H2,1-3H3,(H,19,20)/p-1
SMILES:CC(C)(C)OC(=O)N1CCC(CC1)(c1ccccc1)C(=O)[O-]
Synonyms:
  • 1-(tert-butoxycarbonyl)-4-PHENYL-4-piperidinecarboxylic acid
  • 4-PHENYL-PIPERIDINE-1,4-Dicarboxylic acid MONO-TERT-BUTYL ESTER
  • Rarechem Em Wb 0182
  • N-BOC-4-PHENYL-4-piperidinecarboxylic acid
  • 1-(Tert-Butoxycarbonyl)-4-Phenylpiperidine-4-Carboxylic Acid
  • 1-(Tert-Butoxycarbonyl)-4-Phenylpiperidine-4-Carboxylate
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