CAS 34573-74-5
:2,6-Piperidinedione, 3-methylene-
Description:
2,6-Piperidinedione, 3-methylene- is a chemical compound characterized by its piperidine ring structure, which features two carbonyl (C=O) groups at the 2 and 6 positions and a methylene (-CH2-) group at the 3 position. This compound is typically a solid at room temperature and is soluble in polar organic solvents. It exhibits properties typical of diketones, including the ability to participate in various chemical reactions such as nucleophilic addition and condensation. The presence of the piperidine ring contributes to its potential biological activity, making it of interest in medicinal chemistry. Additionally, the compound may exhibit tautomeric forms due to the keto-enol equilibrium, influencing its reactivity and stability. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if inhaled or ingested. Overall, 2,6-Piperidinedione, 3-methylene- is a versatile compound with applications in research and potential pharmaceutical development.
Formula:C6H7NO2
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Found 1 products.
3-Methylidenepiperidine-2,6-dione
CAS:<p>3-Methylidenepiperidine-2,6-dione is an unsaturated compound that has been isolated from coal tar. It is a colorless solid that melts at temperatures between 200 and 220 degrees Celsius. 3-Methylidenepiperidine-2,6-dione has been shown to be aliphatic and inorganic in nature. It is soluble in water, but insoluble in ether or chloroform. 3-Methylidenepiperidine-2,6-dione reacts with acid to form a cyclic dinitrile that hydrolyzes to form an organic acid (e.g., glutarimide) and diamide. The reaction is more pronounced when the concentration of acid is increased and when the pH of the solution is neutralized with a base such as sodium hydroxide or potassium hydroxide. 3-Methylidenepiperidine-2,6-dione also preferentially hydrolyzes d</p>Formula:C6H7NO2Purity:Min. 95%Molecular weight:125.13 g/mol
