4-Methyl-4-(2-methylpropyl)piperidine-2,6-dione, also known by its CAS number 50849-39-3, is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features two carbonyl groups (ketones) at the 2 and 6 positions of the piperidine ring, contributing to its diketone classification. The presence of a methyl group at the 4 position and a branched alkyl group (2-methylpropyl) at the same position enhances its steric bulk and may influence its reactivity and solubility. Typically, compounds of this nature can exhibit various biological activities, making them of interest in medicinal chemistry. The physical properties, such as melting point, boiling point, and solubility, would depend on the specific molecular interactions and the overall structure. Additionally, the compound may participate in various chemical reactions, including nucleophilic additions and cyclization, due to the electrophilic nature of the carbonyl groups. Its applications could range from pharmaceuticals to agrochemicals, depending on its biological activity and chemical reactivity.

4-methyl-4-(2-methylpropyl)piperidine-2,6-dione

50849-39-3: 4-Methyl-4-(2-methylpropyl)piperidine-2,6-dione, also known by its CAS number 50849-39-3, is a chemical compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features two carbonyl groups (ketones) at the 2 and 6 positions of the piperidine ring, contributing to its diketone classification. The presence of a methyl group at the 4 position and a branched alkyl group (2-methylpropyl) at the same position enhances its steric bulk and may influence its reactivity and solubility. Typically, compounds of this nature can exhibit various biological activities, making them of interest in medicinal chemistry. The physical properties, such as melting point, boiling point, and solubility, would depend on the specific molecular interactions and the overall structure. Additionally, the compound may participate in various chemical reactions, including nucleophilic additions and cyclization, due to the electrophilic nature of the carbonyl groups. Its applications could range from pharmaceuticals to agrochemicals, depending on its biological activity and chemical reactivity.

CAS 50849-39-3

4-methyl-4-(2-methylpropyl)piperidine-2,6-dione

4-Methyl-4-(2-methylpropyl)piperidine-2,6-dione

Ref: 3D-ACA84939