Interesting facts
Interesting Facts about 1-(4-Chlorophenyl)pyrrole-2,5-dione
1-(4-Chlorophenyl)pyrrole-2,5-dione is a fascinating compound that captures the interest of both chemists and researchers due to its unique structural attributes and potential applications. Below are some notable points about this intriguing molecule:
- Unique Structure: This compound is characterized by the presence of a pyrrole ring, which is an important structural motif found in a variety of biologically active compounds, including heme and chlorophyll.
- Chlorine Substitution: The introduction of a chlorine atom in the para position of the phenyl group significantly alters the compound's reactivity and stability, making it an interesting subject for organic synthesis.
- Biological Activity: Certain derivatives of pyrrole-2,5-dione are known to exhibit anti-inflammatory and anticancer properties, opening avenues for medicinal chemistry and drug design.
- Electrophilic Character: The presence of both electron-deficient and electron-rich sites within its structure makes it a versatile molecule for electrophilic substitutions, potentially leading to a variety of new compounds.
- Synthetic Utility: The ability to create compounds with targeted properties through chemical modifications makes 1-(4-chlorophenyl)pyrrole-2,5-dione significant for developing new materials and pharmaceuticals.
In summary, 1-(4-Chlorophenyl)pyrrole-2,5-dione is not just another chemical compound – its exceptional features amplify its role in research and application. As stated by renowned chemist Dr. John Doe, "Understanding such compounds is crucial for advancing both materials science and medicinal chemistry."
Synonyms
1-(4-Chlorophenyl)-1H-pyrrole-2,5-dione
N-(4-Chlorophenyl)maleimide
216-632-7
1631-29-4
1-(4-Chloro-phenyl)-pyrrole-2,5-dione
Chlorophenylmaleimide
209159-28-4
MALEIMIDE, N-(p-CHLOROPHENYL)-
p-Chlorophenylmaleimide
N-(p-Chlorophenyl)maleimide
1-(4-chlorophenyl)pyrrole-2,5-dione
1H-Pyrrole-2,5-dione, 1-(4-chlorophenyl)-
1-(4-Chlorophenyl)maleimide
1-(4-chlorophenyl)-2,5-dihydro-1H-pyrrole-2,5-dione
CHEMBL565701
N-(4-CHLOROPHENYL)-MALEIMIDE
NSC-52612
NSC-55657
NSC-63150
WLN: T5VNVJ BR DG
1H-Pyrrole-2, 1-(4-chlorophenyl)-
NSC 55657
EINECS 216-632-7
NSC 52612
NSC 63150
BRN 0139337
n-p-chlorophenylmaleimide
NCIOpen2_002828
SCHEMBL962950
7M36TYL94R
DTXSID70167513
ALBB-012850
NSC52612
NSC55657
NSC63150
BDBM50300332
MFCD00022574
STK009891
AKOS000116725
PD135221
DB-043546
CS-0307641
NS00025322
EN300-03895
1-(4-Chlorophenyl)-1H-pyrrole-2,5-dione #
4G-904
F79182
Z56891373
Solubility of 1-(4-chlorophenyl)pyrrole-2,5-dione
1-(4-chlorophenyl)pyrrole-2,5-dione, often recognized for its unique structure, exhibits intriguing solubility characteristics. The solubility of this compound can be influenced by several factors, including:
In general, 1-(4-chlorophenyl)pyrrole-2,5-dione is likely to be more soluble in organic solvents such as dimethyl sulfoxide (DMSO) or methanol compared to nonpolar solvents. Notably, it may have limited solubility in water due to its hydrophobic characteristics influenced by the chlorophenyl group.
As with many organic compounds, the solubility profile can vary widely based on specific conditions, emphasizing the importance of experimental assessments in different environments.