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57037-95-3

2-(4-AMINOPHENYL)-6-NITRO-1H-BENZO[DE]ISOQUINOLINE-1,3(2H)-DIONE

Catalog#: AR00EO00  |   CAS#: 57037-95-3  |   MDL#: MFCD03950769  |   MF: C18H11N3O4  |   MW: 333.2976

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Catalog Number AR00EO00
Chemical Name 2-(4-AMINOPHENYL)-6-NITRO-1H-BENZO[DE]ISOQUINOLINE-1,3(2H)-DIONE
CAS Number 57037-95-3
Molecular Formula C18H11N3O4
Molecular Weight 333.2976
MDL Number MFCD03950769
SMILES Nc1ccc(cc1)n1c(=O)c2cccc3c2c(c1=O)ccc3[N+](=O)[O-]

As a chemist, I understand the significance of 2-(4-Aminophenyl)-6-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione in chemical synthesis. This compound plays a crucial role as a building block in organic chemistry reactions, particularly in the synthesis of diverse heterocyclic compounds. Its unique structural features make it a valuable component for creating complex molecular structures with specific properties and functions.In chemical synthesis, 2-(4-Aminophenyl)-6-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione serves as a versatile intermediate that can undergo various transformations to yield a wide range of derivatives. Its amino and nitro functional groups provide key sites for further derivatization, allowing for the introduction of different substituents or functional moieties to tailor the compound for specific applications.Furthermore, the presence of the benzo[de]isoquinoline scaffold in this molecule offers opportunities for the construction of polycyclic frameworks with enhanced structural complexity. By leveraging the reactivity of the nitro group and the amino group, chemists can orchestrate strategic synthetic pathways to access novel compounds with potential biological activities or material properties.Overall, the application of 2-(4-Aminophenyl)-6-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione in chemical synthesis opens up avenues for designing and synthesizing diverse organic molecules with tailored structures and properties, making it a valuable tool for researchers in synthetic chemistry and drug discovery.
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