2-(Dimethoxymethyl)-1,8-naphthyridine is a chemical compound characterized by its naphthyridine core, which is a bicyclic structure containing nitrogen atoms. This compound features two methoxy groups attached to a methylene bridge, contributing to its unique reactivity and solubility properties. Typically, naphthyridines exhibit interesting biological activities, making them of interest in medicinal chemistry. The presence of the dimethoxymethyl substituent can enhance lipophilicity, potentially influencing the compound's pharmacokinetics and interaction with biological targets. The molecular structure suggests that it may participate in hydrogen bonding and other intermolecular interactions due to the presence of the nitrogen atom and the methoxy groups. Additionally, the compound may exhibit fluorescence properties, which can be useful in various applications, including imaging and sensing. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 2-(dimethoxymethyl)-1,8-naphthyridine represents a versatile structure with potential applications in pharmaceuticals and materials science.

2-(dimethoxymethyl)-1,8-naphthyridine

204452-90-4: 2-(Dimethoxymethyl)-1,8-naphthyridine is a chemical compound characterized by its naphthyridine core, which is a bicyclic structure containing nitrogen atoms. This compound features two methoxy groups attached to a methylene bridge, contributing to its unique reactivity and solubility properties. Typically, naphthyridines exhibit interesting biological activities, making them of interest in medicinal chemistry. The presence of the dimethoxymethyl substituent can enhance lipophilicity, potentially influencing the compound's pharmacokinetics and interaction with biological targets. The molecular structure suggests that it may participate in hydrogen bonding and other intermolecular interactions due to the presence of the nitrogen atom and the methoxy groups. Additionally, the compound may exhibit fluorescence properties, which can be useful in various applications, including imaging and sensing. As with many organic compounds, its stability, solubility, and reactivity can be influenced by environmental factors such as pH and temperature. Overall, 2-(dimethoxymethyl)-1,8-naphthyridine represents a versatile structure with potential applications in pharmaceuticals and materials science.

CAS 204452-90-4

2-(dimethoxymethyl)-1,8-naphthyridine

2-Dimethoxymethyl-[1,8]naphthyridine

Ref: IN-DA0029HV

2-(Dimethoxymethyl)-1,8-naphthyridine

Ref: 10-F219905