CAS 306296-67-3
:prop-2-en-1-yl 4-oxopiperidine-1-carboxylate
Description:
Prop-2-en-1-yl 4-oxopiperidine-1-carboxylate, with the CAS number 306296-67-3, is an organic compound characterized by its unique structure that includes a piperidine ring, a carboxylate group, and an allylic double bond. This compound typically exhibits properties associated with both its piperidine and carboxylate functionalities, such as moderate polarity and potential for hydrogen bonding. The presence of the double bond suggests reactivity typical of alkenes, allowing for various chemical transformations, including polymerization and addition reactions. Additionally, the 4-oxo group indicates the presence of a carbonyl functionality, which can influence the compound's reactivity and stability. This compound may be of interest in synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals, due to its potential biological activity and versatility in chemical reactions. Its solubility and stability would depend on the specific conditions, such as solvent choice and temperature.
Formula:C9H13NO3
InChI:InChI=1/C9H13NO3/c1-2-7-13-9(12)10-5-3-8(11)4-6-10/h2H,1,3-7H2
SMILES:C=CCOC(=O)N1CCC(=O)CC1
Synonyms:- 1-Piperidinecarboxylic acid, 4-oxo-, 2-propen-1-yl ester
- Allyl 4-oxopiperidine-1-carboxylate
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Found 4 products.
Allyl 4-oxopiperidine-1-carboxylate
CAS:Formula:C9H13NO3Purity:95%Color and Shape:LiquidMolecular weight:183.20441-N-Alloc-4-piperidone
CAS:Formula:C9H13NO3Purity:95%Color and Shape:Liquid, ClearMolecular weight:183.207N-Allyloxycarbonyl-4-piperidone
CAS:Controlled ProductFormula:C9H13NO3Color and Shape:NeatMolecular weight:183.204



