4-Bromo-5-(pyrrolidin-1-yl)pyridazin-3(2H)-one is a chemical compound characterized by its pyridazine core, which is a six-membered aromatic ring containing two nitrogen atoms. The presence of a bromine atom at the 4-position and a pyrrolidine moiety at the 5-position contributes to its unique properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The pyrrolidine group may enhance interactions with biological targets, while the bromine substituent can influence the compound's reactivity and lipophilicity. Additionally, the compound may exhibit specific spectral characteristics in techniques such as NMR and mass spectrometry, aiding in its identification and characterization. Overall, 4-bromo-5-(pyrrolidin-1-yl)pyridazin-3(2H)-one represents a versatile scaffold for further chemical modifications and potential applications in drug discovery.

4-bromo-5-(pyrrolidin-1-yl)pyridazin-3(2H)-one

692749-93-2: 4-Bromo-5-(pyrrolidin-1-yl)pyridazin-3(2H)-one is a chemical compound characterized by its pyridazine core, which is a six-membered aromatic ring containing two nitrogen atoms. The presence of a bromine atom at the 4-position and a pyrrolidine moiety at the 5-position contributes to its unique properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential biological activity, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The pyrrolidine group may enhance interactions with biological targets, while the bromine substituent can influence the compound's reactivity and lipophilicity. Additionally, the compound may exhibit specific spectral characteristics in techniques such as NMR and mass spectrometry, aiding in its identification and characterization. Overall, 4-bromo-5-(pyrrolidin-1-yl)pyridazin-3(2H)-one represents a versatile scaffold for further chemical modifications and potential applications in drug discovery.

CAS 692749-93-2

4-bromo-5-(pyrrolidin-1-yl)pyridazin-3(2H)-one

4-Bromo-5-(1-pyrrolidinyl)-3(2h)-pyridazinone

Ref: IN-DA00FD97

4-bromo-5-(1-pyrrolidinyl)-3(2H)-pyridazinone

Ref: 10-F311109