3-Chloro-5-methoxypyridazine is a heterocyclic organic compound characterized by its pyridazine ring, which is a six-membered aromatic ring containing two adjacent nitrogen atoms. The presence of a chlorine atom at the 3-position and a methoxy group (-OCH3) at the 5-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its structure suggests potential reactivity due to the electron-withdrawing nature of the chlorine atom and the electron-donating properties of the methoxy group, which can influence its behavior in chemical reactions. 3-Chloro-5-methoxypyridazine may be of interest in pharmaceutical research and development, particularly for its potential biological activities. As with many chemical substances, safety precautions should be observed when handling it, as it may pose health risks or environmental hazards. Proper storage and disposal methods are essential to mitigate any potential risks associated with its use.

3-Chloro-5-methoxypyridazine

123696-02-6: Pyridazine, 3-Chloro-5-Methoxy-, 3-Chloro-5-methoxypyridazine

Pyridazine, 3-chloro-5-methoxy-

3-Chloro-5-methoxypyridazine is an organic compound with the formula CHClNOS. It is a white solid that is soluble in water. The compound has been used as a target for hydrogenation, which produces the target compound 3,5-dimethoxybenzaldehyde. This reaction can be catalyzed by phosphorous and requires a hydrogenation catalyst such as platinum or palladium. The product of this reaction can be monitored using gas chromatography and mass spectroscopy to confirm the conversion of 3-chloro-5-methoxypyridazine to 3,5-dimethoxybenzaldehyde.

CAS 123696-02-6: 3-Chloro-5-methoxypyridazine

Pyridazine, 3-chloro-5-methoxy-

Ref: IN-DA000KY1

3-Chloro-5-methoxypyridazine

Ref: 54-OR903747

3-Chloro-5-methoxypyridazine

Ref: 10-F093603

3-Chloro-5-methoxypyridazine

Ref: 3D-FC46391