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CAS 91419-48-6

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tert-butyl 4-(aminocarbonyl)tetrahydropyridine-1(2H)-carboxylate

Description:
Tert-butyl 4-(aminocarbonyl)tetrahydropyridine-1(2H)-carboxylate, identified by its CAS number 91419-48-6, is a chemical compound that features a tetrahydropyridine ring, which is a saturated six-membered ring containing one nitrogen atom. This compound is characterized by the presence of a tert-butyl ester group, which enhances its lipophilicity and stability. The aminocarbonyl functional group indicates the presence of an amine and a carbonyl group, contributing to its potential reactivity and ability to participate in various chemical reactions, such as amide formation. The carboxylate moiety suggests that it can act as a weak acid, and its structure may allow for hydrogen bonding interactions. This compound may be of interest in medicinal chemistry and organic synthesis due to its potential biological activity and utility as a building block in the synthesis of more complex molecules. As with many organic compounds, its physical properties, such as solubility and melting point, would depend on the specific conditions and purity of the sample.
Formula:C11H20N2O3
InChI:InChI=1/C11H20N2O3/c1-11(2,3)16-10(15)13-6-4-8(5-7-13)9(12)14/h8H,4-7H2,1-3H3,(H2,12,14)
SMILES:CC(C)(C)OC(=O)N1CCC(CC1)C(=N)O
Synonyms:
  • 1-Piperidinecarboxylic acid, 4-(aminocarbonyl)-, 1,1-dimethylethyl ester
  • 1-tert-Butoxycarbonylpiperidine-4-carboxamide
  • Tert-Butyl 4-Carbamoylpiperidine-1-Carboxylate
  • 1-N-Boc-Piperidine-4-Carboxamide
  • N-Boc-4-Piperidinecarboxamide
  • 1-Boc-4-Piperidine carboxamide
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