CAS 358969-71-8
:prop-2-en-1-yl 4-aminopiperidine-1-carboxylate
Description:
Prop-2-en-1-yl 4-aminopiperidine-1-carboxylate, identified by its CAS number 358969-71-8, is a chemical compound that features a piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle. This compound is characterized by the presence of an amino group and a carboxylate functional group, contributing to its potential as a bioactive molecule. The prop-2-en-1-yl group indicates that it has an allylic double bond, which can participate in various chemical reactions, such as polymerization or addition reactions. The structural features suggest that it may exhibit interesting pharmacological properties, making it a candidate for research in medicinal chemistry. Additionally, the presence of both the amino and carboxylate groups may influence its solubility and reactivity, impacting its behavior in biological systems. Overall, prop-2-en-1-yl 4-aminopiperidine-1-carboxylate is a compound of interest in the fields of organic synthesis and drug development due to its unique structural characteristics.
Formula:C9H16N2O2
InChI:InChI=1/C9H16N2O2/c1-2-7-13-9(12)11-5-3-8(10)4-6-11/h2,8H,1,3-7,10H2
SMILES:C=CCOC(=O)N1CCC(CC1)N
Synonyms:- 1-Piperidinecarboxylic acid, 4-amino-, 2-propen-1-yl ester
- Allyl 4-aminopiperidine-1-carboxylate
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Allyl 4-Aminopiperdine-1-carboxylate
CAS:Controlled Product<p>Applications Allyl 4-Aminopiperdine-1-carboxylate has been used as a reactant for the preparation of 4-aminopiperdine analogs.<br>References Fernandez-Forner, D., et. al. Tetrahedron Lett., 42, 4471 (2001)<br></p>Formula:C9H16N2O2Color and Shape:NeatMolecular weight:184.24
