CAS 73926-98-4

1-(4-Methoxyphenyl)-3-methylene-2,5-pyrrolidinedione

Description:

1-(4-Methoxyphenyl)-3-methylene-2,5-pyrrolidinedione, also known by its CAS number 73926-98-4, is a synthetic organic compound characterized by its unique pyrrolidine structure. This compound features a methylene bridge connecting a pyrrolidinedione moiety to a para-methoxyphenyl group, contributing to its potential biological activity. It typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its non-polar characteristics. The presence of the methoxy group enhances its lipophilicity, which may influence its interaction with biological systems. This compound is of interest in medicinal chemistry due to its potential pharmacological properties, including anti-inflammatory and analgesic effects. Its reactivity can be attributed to the electrophilic nature of the methylene group, which may participate in various chemical reactions. As with many organic compounds, safety precautions should be observed when handling it, as its biological effects and toxicity profiles require further investigation. Overall, 1-(4-Methoxyphenyl)-3-methylene-2,5-pyrrolidinedione represents a fascinating subject for research in drug development and organic synthesis.

Formula: C₁₂H₁₁NO₃

InChI: InChI=1S/C12H11NO3/c1-8-7-11(14)13(12(8)15)9-3-5-10(16-2)6-4-9/h3-6H,1,7H2,2H3

InChI key: InChIKey=WBDXCBZSLZXLCT-UHFFFAOYSA-N

SMILES: O=C1N(C(=O)C(=C)C1)C2=CC=C(OC)C=C2

Synonyms:

• N-(p-Methoxyphenyl)itaconimide
• 1-(4-Methoxyphenyl)-3-methylene-2,5-pyrrolidinedione
• 2,5-Pyrrolidinedione, 1-(4-methoxyphenyl)-3-methylene-
• Succinimide, N-(p-methoxyphenyl)-2-methylene-
• NSC 222702