[1]Benzofuro[2,3-d]pyridazin-4(3H)-one, with the CAS number 50266-85-8, is a heterocyclic organic compound characterized by its fused ring structure, which includes a benzofuran moiety and a pyridazinone. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry and pharmacology. Its structure contributes to its potential as a scaffold for drug development, particularly in targeting various biological pathways. The presence of the pyridazinone ring often imparts stability and influences the compound's reactivity and solubility. Additionally, [1]benzofuro[2,3-d]pyridazin-4(3H)-one may exhibit fluorescence properties, which can be useful in analytical applications. The compound's synthesis usually involves multi-step organic reactions, and its derivatives may be explored for enhanced efficacy or reduced toxicity in therapeutic contexts. As with many heterocycles, the specific interactions and mechanisms of action are subjects of ongoing research, highlighting its relevance in the field of organic and medicinal chemistry.

[1]benzofuro[2,3-d]pyridazin-4(3H)-one

50266-85-8: [1]Benzofuro[2,3-d]pyridazin-4(3H)-one, with the CAS number 50266-85-8, is a heterocyclic organic compound characterized by its fused ring structure, which includes a benzofuran moiety and a pyridazinone. This compound typically exhibits a range of biological activities, making it of interest in medicinal chemistry and pharmacology. Its structure contributes to its potential as a scaffold for drug development, particularly in targeting various biological pathways. The presence of the pyridazinone ring often imparts stability and influences the compound's reactivity and solubility. Additionally, [1]benzofuro[2,3-d]pyridazin-4(3H)-one may exhibit fluorescence properties, which can be useful in analytical applications. The compound's synthesis usually involves multi-step organic reactions, and its derivatives may be explored for enhanced efficacy or reduced toxicity in therapeutic contexts. As with many heterocycles, the specific interactions and mechanisms of action are subjects of ongoing research, highlighting its relevance in the field of organic and medicinal chemistry.

CAS 50266-85-8

[1]benzofuro[2,3-d]pyridazin-4(3H)-one

benzofuro[2,3-d]pyridazin-4(3H)-one

Ref: 54-OR307759