CAS 85547-22-4
:8,9-Dimethoxy-1H-benzo[de][1,6]naphthyridine
Description:
8,9-Dimethoxy-1H-benzo[de][1,6]naphthyridine is a heterocyclic organic compound characterized by its fused ring structure, which incorporates both benzene and naphthyridine moieties. This compound features two methoxy groups (-OCH3) attached to the 8 and 9 positions of the naphthyridine ring, which can influence its chemical reactivity and solubility. The presence of these methoxy groups typically enhances the compound's lipophilicity and may affect its biological activity, making it of interest in medicinal chemistry. The compound's structure suggests potential applications in pharmaceuticals, particularly in the development of agents targeting specific biological pathways. Additionally, its unique arrangement of nitrogen and carbon atoms contributes to its electronic properties, which can be explored in various chemical reactions. As with many heterocycles, the stability and reactivity of 8,9-Dimethoxy-1H-benzo[de][1,6]naphthyridine can be influenced by environmental factors such as pH and solvent polarity. Overall, this compound represents a fascinating area of study within organic and medicinal chemistry.
Formula:C13H12N2O2
InChI:InChI=1/C13H12N2O2/c1-16-10-7-8-3-5-14-9-4-6-15-12(11(8)9)13(10)17-2/h3-7,15H,1-2H3
InChI key:InChIKey=IVXSXOFPZFVZTM-UHFFFAOYSA-N
SMILES:O(C)C1=C2C3=C(C=C1OC)C=CN=C3C=CN2
Synonyms:- 1H-benzo[de][1,6]naphthyridine, 8,9-dimethoxy-
- Aaptamine
- 8,9-dimethoxy-1H-benzo[de]-1,6-naphthyridine
- 8,9-Dimethoxy-1H-benzo[de][1,6]naphthyridine
- 8,9-Dimethoxy-1H-benzo[de][1,6]naphthyridine
- 6]naphtyridine
- 8;9-DIMETHOXY-1H-BENZO[DE][1;6]NAPHTYRIDINE
- 9-Dimethoxy-1H-benzo[de][1
- 6)naphthyridine,8,9-dimethoxy-1h-benzo(de)(
- Apatamine
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Found 4 products.
Aaptamine
CAS:<p>Aaptamine functions as a proteasome inhibitor, it activates p21 promoter in a p53-independent manner.</p>Formula:C13H12N2O2Purity:98%Color and Shape:SolidMolecular weight:228.25



