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CAS 146667-84-7

:

3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester

Description:
3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester, with the CAS number 146667-84-7, is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features a tert-butyl ester functional group, contributing to its hydrophobic properties, while the hydroxyethyl substituent enhances its solubility in polar solvents. The presence of the carboxylic acid moiety indicates potential for hydrogen bonding and reactivity, making it useful in various chemical reactions, including esterification and amidation. Its structural features suggest applications in medicinal chemistry, particularly in the development of pharmaceuticals, where it may serve as a building block or intermediate. Additionally, the compound's ability to form salts with bases can influence its bioavailability and pharmacokinetics. Overall, 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester is a versatile compound with significant implications in organic synthesis and drug development.
Formula:C12H23NO3
InChI:InChI=1/C12H23NO3/c1-12(2,3)16-11(15)13-7-4-5-10(9-13)6-8-14/h10,14H,4-9H2,1-3H3
SMILES:CC(C)(C)OC(=O)N1CCCC(CCO)C1
Synonyms:
  • 3-(2-Hydroxy-Ethyl)-Piperidine-1-Carboxylic Acid Tert-Butyl Ester
  • 1-N-Boc-Piperidine-3-Ethanol
  • 1-Boc-3-(2-Hydroxy-Ethyl)-Piperidine
  • Tert-Butyl 3-(2-Hydroxyethyl)Piperidine-1-Carboxylate
  • 1-Boc-3-hydroxyethyl piperidine
  • 3-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl es...
  • N-Boc-3-(2-hydroxyethyl)piperidine
  • 1-Piperidinecarboxylic acid, 3-(2-hydroxyethyl)-, 1,1-dimethylethyl ester
  • 1-N-Boc-piperidine-3-ethanol ,98%
  • 1-Boc-piperidine-3-ethanol
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