CAS 17825-86-4

3,4-dimethylpyrrole-2,5-dione

Description:

3,4-Dimethylpyrrole-2,5-dione, also known as 3,4-dimethyl-2,5-pyrrolidinedione, is an organic compound characterized by its pyrrole ring structure with two methyl groups at the 3 and 4 positions and two carbonyl groups at the 2 and 5 positions. This compound is a derivative of pyrrole, which is a five-membered aromatic heterocycle containing nitrogen. The presence of the carbonyl groups contributes to its reactivity, making it a potential candidate for various chemical reactions, including cycloadditions and nucleophilic substitutions. It is typically a solid at room temperature and may exhibit solubility in polar organic solvents. The compound's unique structure allows it to participate in biological processes and may have applications in pharmaceuticals or as a building block in organic synthesis. Additionally, its properties can be influenced by the presence of substituents, which can affect its stability, reactivity, and interaction with other molecules. Safety data should be consulted for handling and usage, as with any chemical substance.

Formula: C₆H₇NO₂

InChI: InChI=1/C6H7NO2/c1-3-4(2)6(9)7-5(3)8/h1-2H3,(H,7,8,9)

SMILES: CC1=C(C)C(=O)N=C1O

Synonyms:

• 2,3-Dimethylmaleimide
• 3,4-dimethyl-1H-pyrrole-2,5-dione

3,4-dimethyl-2,5-dihydro-1H-pyrrole-2,5-dione

CAS: 17825-86-4

Formula: C₆H₇NO₂

Molecular weight: 125.1253

Ref: IN-DA0025V9

3,4-Dimethyl-2,5-dihydro-1H-pyrrole-2,5-dione

CAS: 17825-86-4

3,4-Dimethyl-2,5-dihydro-1H-pyrrole-2,5-dione is an oxidation product of 2,6-dimethylphenol. It has been shown to crosslink with a matrix polymer and can be used as a bioconjugate in the synthesis of polymers. 3,4-Dimethyl-2,5-dihydro-1H-pyrrole-2,5-dione can react with nitric acid to form nitro groups and it can be used for coating plates or other objects. This compound is also susceptible to UV irradiation and organic solvents.

Formula: C₆H₇NO₂

Purity: Min. 95%

Molecular weight: 125.13 g/mol

Ref: 3D-SAA82586