CAS 13480-36-9
:2,6-Morpholinedione, 4-methyl-
Description:
2,6-Morpholinedione, 4-methyl- is an organic compound characterized by its morpholine ring structure, which contains both nitrogen and oxygen atoms. This compound features two carbonyl groups (C=O) at the 2 and 6 positions of the morpholine ring, contributing to its dione classification. The presence of a methyl group at the 4-position adds to its molecular complexity and influences its chemical reactivity and physical properties. Typically, such compounds exhibit moderate solubility in polar solvents due to the presence of the nitrogen atom, which can engage in hydrogen bonding. The compound may also display biological activity, making it of interest in pharmaceutical and medicinal chemistry. Its stability and reactivity can be influenced by the functional groups present, and it may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices.
Formula:C5H7NO3
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Found 4 products.
4-Methylmorpholine-2,6-dione
CAS:Formula:C5H7NO3Purity:97%Color and Shape:SolidMolecular weight:129.11404-Methylmorpholine-2,6-Dione
CAS:<p>4-Methylmorpholine-2,6-Dione</p>Purity:99%Molecular weight:129.11g/mol4-methylmorpholine-2,6-dione
CAS:Formula:C5H7NO3Purity:95%Color and Shape:SolidMolecular weight:129.1154-Methylmorpholine-2,6-dione
CAS:<p>4-Methylmorpholine-2,6-dione is a ligand that has been used in the synthesis of boronic acid derivatives. It has also been used to activate boronic acids. 4-Methylmorpholine-2,6-dione can be synthesised by reacting aryl boronic acids with dimethylformamide and acetonitrile in the presence of dehydrogenase and a metal catalyst. The resulting product is then cross-coupled with an amine to form the desired conjugate. 4-Methylmorpholine-2,6-dione is unreactive towards dehydration or morpholine.</p>Formula:C5H7NO3Purity:Min. 95%Molecular weight:129.11 g/mol



