
CAS 857190-11-5
:1-(2-propyn-1-yl)-4-piperidinone
Description:
1-(2-Propyn-1-yl)-4-piperidinone, with the CAS number 857190-11-5, is a chemical compound characterized by its piperidinone structure, which features a piperidine ring substituted with a propynyl group. This compound typically exhibits properties associated with both piperidine derivatives and alkynes, including potential basicity due to the nitrogen atom in the piperidine ring. It may also display reactivity characteristic of alkynes, such as undergoing addition reactions. The presence of the carbonyl group in the piperidinone structure suggests it may participate in nucleophilic addition reactions. This compound is of interest in medicinal chemistry and organic synthesis, potentially serving as a building block for more complex molecules. Its solubility and stability can vary depending on the solvent and environmental conditions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken. Overall, 1-(2-propyn-1-yl)-4-piperidinone represents a versatile compound with applications in various chemical research fields.
- 1-(Prop-2-yn-1-yl)piperidin-4-one
- 4-Piperidinone, 1-(2-propyn-1-yl)-
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Found 4 products.
1-(2-Propyn-1-yl)-4-piperidinone
CAS:Formula:C8H11NOPurity:95%Color and Shape:LiquidMolecular weight:137.17901-(Prop-2-yn-1-yl)piperidin-4-one
CAS:1-(Prop-2-yn-1-yl)piperidin-4-onePurity:95%Molecular weight:137.18g/mol1-(2-propyn-1-yl)-4-piperidinone
CAS:Formula:C8H11NOPurity:95%Color and Shape:SolidMolecular weight:137.1821-(Prop-2-yn-1-yl)piperidin-4-one
CAS:1-(Prop-2-yn-1-yl)piperidin-4-one is an anticancer agent that exhibits apoptotic activity in cancer cells. It is a covalent inhibitor of DNA polymerase, which is involved in the synthesis of DNA and RNA. 1-(Prop-2-yn-1-yl)piperidin-4-one inhibits the growth of cancer cells by binding to the active site of DNA polymerase and preventing its function. This drug has been shown to be effective against a range of cancer cell lines including breast, lung, prostate, and bladder cancers. 1-(Prop-2-yn-1-yl)piperidin-4-one also has antiangiogenic effects that may contribute to its anticancer activity.Formula:C8H11NOPurity:Min. 95%Molecular weight:137.17 g/mol



