1-(pyren-1-yl)-1H-pyrrole-2,5-dione
$200.00
CAS No.: 42189-56-0
Catalog No.: WLZ1822
Purity: 95%
MF: C20H11NO2
MW: 297.313
Storage: 2-8 degree Celsius
SMILES: C1(=CC=C2C=CC3=CC=CC4=CC=C1C2=C34)N3C(C=CC3=O)=O
Catalog No.: WLZ1822
Purity: 95%
MF: C20H11NO2
MW: 297.313
Storage: 2-8 degree Celsius
SMILES: C1(=CC=C2C=CC3=CC=CC4=CC=C1C2=C34)N3C(C=CC3=O)=O
CAS NO.: 42189-56-0; 1-(pyren-1-yl)-1H-pyrrole-2,5-dione. PROPERTIES: This pyrroledione derivative features a pyrene group attached to a pyrrole-2,5-dione framework, creating a molecule with potential applications in organic synthesis and materials science. The 1-(pyren-1-yl)-1H-pyrrole-2,5-dione typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes a rigid pyrene system and a pyrroledione moiety that influence the electronic properties and fluorescence characteristics of the molecule. For optimal stability and to prevent degradation, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 1-(pyren-1-yl)-1H-pyrrole-2,5-dione serves as a valuable intermediate in the synthesis of complex organic molecules and materials with specific optical and electronic properties. The pyrene group provides a handle for further functionalization through reactions such as Diels-Alder cycloaddition. In materials science, this compound functions as a building block for creating fluorescent probes and sensors where the unique electronic structure contributes to photoluminescent properties. Additionally, the molecule finds utility in organic electronics as a component of light-emitting diodes (OLEDs) and other optoelectronic devices. Researchers utilizing this compound benefit from its defined structural features, enabling the development of advanced materials with tailored optical and electronic characteristics.
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