Interesting facts
Exploring 1-(p-tolyl)pyrrole-2,5-dione
1-(p-tolyl)pyrrole-2,5-dione is a fascinating compound that draws interest from both organic chemists and materials scientists. This compound belongs to the family of pyrrole derivatives, compounds known for their aromatic properties and diverse applications. Here are some intriguing aspects of 1-(p-tolyl)pyrrole-2,5-dione:
- Origin and Structure: The compound features a pyrrole ring substituted with a p-tolyl group, which enhances its stability and electronic properties. The dual carbonyl groups in the 2 and 5 positions make this structure particularly interesting from a reactivity standpoint.
- Chemical Reactivity: The dione functionality in the structure can act as a versatile site for further chemical modifications. This allows chemists to generate a wide range of derivatives through various functionalization methods, making it an appealing candidate for the development of new materials.
- Potential Applications: Due to its unique electronic characteristics, 1-(p-tolyl)pyrrole-2,5-dione could have promising applications in:
- Organic electronics: It might be utilized in organic semiconductors for various electronic devices.
- Fluorescent materials: The compound's light-emitting properties can open avenues for its use in display technologies.
- Pharmaceutical chemistry: Investigating its bioactivity can lead to new drug candidates.
- Research Interest: The synthesis and study of pyrrole derivatives, including 1-(p-tolyl)pyrrole-2,5-dione, form a critical area of research, particularly in synthetic organic chemistry. Studies continue to explore how variations in substituents can impact the properties and reactivity of such compounds.
In summary, the exploration of 1-(p-tolyl)pyrrole-2,5-dione not only enhances our understanding of pyrrole chemistry but also provides potential pathways for innovative applications across various scientific fields. As a student or researcher in chemistry, investigating such compounds can lead to remarkable discoveries and advancements.
Synonyms
N-(4-Methylphenyl)maleimide
1-(p-Tolyl)-1H-pyrrole-2,5-dione
654-866-5
1631-28-3
p-Tolylmaleimide
1-(4-Methylphenyl)-1H-pyrrole-2,5-dione
MALEIMIDE, N-p-TOLYL-
N-p-Tolylmaleimide
1H-Pyrrole-2,5-dione, 1-(4-methylphenyl)-
N-(p-Methylphenyl)maleimide
1-(4-methylphenyl)pyrrole-2,5-dione
N,p-Tolylmaleimide
NSC 13691
IT 510
MFCD00022581
LB7TXV3P6M
N-(para-Tolyl)-maleimide
1-(4-Methylphenyl)maleimide
CHEMBL578795
NSC-13691
1-(4-methylphenyl)-2,5-dihydro-1H-pyrrole-2,5-dione
25989-85-9
1-(4-Methylphenyl)-1{H}-pyrrole-2,5-dione; 1-(p-tolyl)-1H-pyrrole-2,5-dione
1-p-Tolyl-pyrrole-2,5-dione
BRN 0131320
AI3-32933
p Tolylmaleimide
N-4-Tolylmaleimide
Cyto8D6
UNII-LB7TXV3P6M
1H-Pyrrole-2,5-dione,1-(4-methylphenyl)-
WLN: T5VNVJ BR D1
5-21-10-00016 (Beilstein Handbook Reference)
SCHEMBL140025
DTXSID10167512
GLXC-15142
HMS1787F22
ALBB-017479
N-(1-METHYLPHENYL)MALEIMIDE
NSC13691
BDBM50300315
CCG-48277
NSC148146
STK257434
AKOS000116623
1H-Pyrrole-2, 1-(4-methylphenyl)-
FS-1828
NSC-148146
DB-043545
HY-129592
CS-0106816
EN300-03983
1-(4-Methylphenyl)-1{H}-pyrrole-2,5-dione
F73726
SR-01000637832-1
Z56753962
LOQ
Solubility of 1-(p-tolyl)pyrrole-2,5-dione
1-(p-tolyl)pyrrole-2,5-dione is a fascinating compound that displays unique solubility characteristics. Understanding its solubility can help in both research and practical applications. Here are some key points to consider:
In summary, the solubility of 1-(p-tolyl)pyrrole-2,5-dione is influenced by its molecular structure and the choice of solvent. As with many organic compounds, it is essential to mimic real-world conditions to gain a better understanding of its solubility behavior. Remember, water solubility is minimal, and researchers should select solvents accordingly for optimal results.