CAS 25077-26-3

4-Methyl-2,6-piperidinedione

Description:

4-Methyl-2,6-piperidinedione, also known as N-Methyl-2,6-piperidinedione, is a cyclic organic compound characterized by its piperidine ring structure, which contains two carbonyl groups (ketones) at the 2 and 6 positions and a methyl group at the 4 position. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of diketones, such as the ability to participate in various chemical reactions, including nucleophilic additions and condensation reactions. The presence of the piperidine ring contributes to its potential biological activity, making it of interest in medicinal chemistry. Additionally, 4-Methyl-2,6-piperidinedione may serve as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper laboratory practices and safety protocols should be followed when working with this substance.

Formula: C₆H₉NO₂

InChI: InChI=1S/C6H9NO2/c1-4-2-5(8)7-6(9)3-4/h4H,2-3H2,1H3,(H,7,8,9)

InChI key: InChIKey=OTQNZVVDFWNHDO-UHFFFAOYSA-N

SMILES: CC1CC(=O)NC(=O)C1

Synonyms:

• Glutarimide, 3-methyl-
• 4-Methyl-2,6-piperidinedione
• 2,6-Piperidinedione, 4-methyl-
• 3-Methylglutarimide
• NSC 39842

4-Methylpiperidine-2,6-dione

CAS: 25077-26-3

Formula: C₆H₉NO₂

Molecular weight: 127.1412

Ref: IN-DA002QEU

4-Methylpiperidine-2,6-dione

CAS: 25077-26-3

4-Methylpiperidine-2,6-dione is a diacid that is used as an iron chelating agent. It binds to ferric ions and prevents them from reacting with other molecules. The molecular descriptors for 4-methylpiperidine-2,6-dione are acidic ph, piperazine, and chloride. This molecule has been shown to be reactive in predictive models and hydrolyzes in aqueous solutions.

Formula: C₆H₉NO₂

Purity: Min. 95%

Molecular weight: 127.14 g/mol

Ref: 3D-ABA07726