CAS 10495-37-1

4-Amino-N-phenyl-1,8-naphthalimide

Description:

4-Amino-N-phenyl-1,8-naphthalimide is an organic compound characterized by its naphthalimide structure, which features a naphthalene ring fused to an imide functional group. The presence of an amino group and a phenyl substituent enhances its reactivity and solubility in various solvents. This compound typically exhibits strong fluorescence properties, making it useful in applications such as fluorescent probes, dyes, and sensors. Its molecular structure contributes to its photophysical characteristics, including absorption and emission spectra, which can be influenced by the solvent environment. Additionally, 4-Amino-N-phenyl-1,8-naphthalimide may exhibit potential biological activities, including antimicrobial or anticancer properties, although specific biological effects would depend on the context of its use and the conditions of the study. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance. Overall, this compound is of interest in both materials science and medicinal chemistry due to its unique properties and potential applications.

Formula: C₁₈H₁₂N₂O₂

InChI: InChI=1S/C18H12N2O2/c19-15-10-9-14-16-12(15)7-4-8-13(16)17(21)20(18(14)22)11-5-2-1-3-6-11/h1-10H,19H2

InChI key: InChIKey=HRQSPGSEYDLAIM-UHFFFAOYSA-N

SMILES: O=C1C=2C=3C(C(=O)N1C4=CC=CC=C4)=CC=CC3C(N)=CC2

Synonyms:

• 1H-benz[de]isoquinoline-1,3(2H)-dione, 6-amino-2-phenyl-
• 4-Amino-N-phenyl-1,8-naphthalimide
• 4-Amino-N-phenylnaphthalimide
• 4-Aminonaphthalic acid phenylimide
• 6-Amino-2-phenyl-1H-benz[de]isoquinoline-1,3(2H)-dione
• 6-Amino-2-phenyl-benzo[de]isoquinoline-1,3-dione
• Dfp 2
• N-Phenyl-4-amino-1,8-naphthalenedicarboxylateimide
• N-Phenyl-4-aminonaphthalimide
• Naphthalimide, 4-amino-N-phenyl-