2-Piperidinone, 1-propyl- is a cyclic amide characterized by its piperidinone structure, which features a six-membered ring containing one nitrogen atom and a carbonyl group. This compound is classified as a lactam, specifically a substituted piperidinone, where a propyl group is attached to the nitrogen atom of the piperidine ring. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the carbonyl group contributes to its reactivity, making it a potential intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. The compound exhibits moderate solubility in polar solvents due to its polar functional groups, while its hydrophobic propyl chain influences its solubility in non-polar solvents. Additionally, 2-Piperidinone, 1-propyl- may exhibit basic properties due to the nitrogen atom in the ring, allowing it to participate in various chemical reactions, including nucleophilic substitutions and cyclization processes. Safety data should be consulted for handling and exposure guidelines.

2-Piperidinone, 1-propyl-

15865-19-7: 2-Piperidinone, 1-propyl- is a cyclic amide characterized by its piperidinone structure, which features a six-membered ring containing one nitrogen atom and a carbonyl group. This compound is classified as a lactam, specifically a substituted piperidinone, where a propyl group is attached to the nitrogen atom of the piperidine ring. It is typically a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the carbonyl group contributes to its reactivity, making it a potential intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. The compound exhibits moderate solubility in polar solvents due to its polar functional groups, while its hydrophobic propyl chain influences its solubility in non-polar solvents. Additionally, 2-Piperidinone, 1-propyl- may exhibit basic properties due to the nitrogen atom in the ring, allowing it to participate in various chemical reactions, including nucleophilic substitutions and cyclization processes. Safety data should be consulted for handling and exposure guidelines.

CAS 15865-19-7

2-Piperidinone, 1-propyl-

2-Piperidinone, 1-propyl-

Ref: IN-DA001QQF

1-Propylpiperidin-2-ol

Ref: TR-P838515