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CAS 91419-49-7

:

1-Piperidinecarboxylic acid, 3-(aminocarbonyl)-, 1,1-dimethylethyl ester

Description:
1-Piperidinecarboxylic acid, 3-(aminocarbonyl)-, 1,1-dimethylethyl ester, also known by its CAS number 91419-49-7, is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. This compound features a carboxylic acid functional group and an ester linkage, indicating it can participate in various chemical reactions typical of carboxylic acids and esters. The presence of the aminocarbonyl group suggests that it has potential applications in medicinal chemistry, particularly in the synthesis of pharmaceuticals. The tert-butyl ester group provides steric hindrance, which can influence the compound's reactivity and solubility. Generally, compounds of this nature may exhibit biological activity, making them of interest in drug development. Additionally, the compound's stability and solubility in organic solvents can vary based on its functional groups, which is crucial for its application in various chemical processes. Overall, this compound represents a versatile structure with potential utility in organic synthesis and pharmaceutical applications.
Formula:C11H20N2O3
InChI:InChI=1/C11H20N2O3/c1-11(2,3)16-10(15)13-6-4-5-8(7-13)9(12)14/h8H,4-7H2,1-3H3,(H2,12,14)
SMILES:CC(C)(C)OC(=O)N1CCCC(C1)C(=N)O
Synonyms:
  • N-Boc-Nipecotamide
  • Tert-Butyl 3-Carbamoylpiperidine-1-Carboxylate
  • 1-Boc-3-piperidinecarboxamide
  • 1-N-Boc-Piperidine-3-Carboxamide
  • 3-Carbamoyl-Piperidine-1-Carboxylic Acid Tert-Butyl Ester
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