4-Chloro-3,5-dimethoxypyridazine 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 chlorine and methoxy groups at specific positions on the ring significantly influences its chemical properties and reactivity. The chlorine atom, being an electronegative substituent, can enhance the compound's electrophilic character, while the methoxy groups contribute to its overall electron-donating ability, affecting its solubility and interaction with other molecules. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its structure allows for potential applications in agrochemicals or as intermediates in organic synthesis. The compound is typically stable under standard conditions but may undergo reactions such as nucleophilic substitution or electrophilic aromatic substitution depending on the reaction environment. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

4-chloro-3,5-dimethoxypyridazine

63910-48-5: 4-Chloro-3,5-dimethoxypyridazine 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 chlorine and methoxy groups at specific positions on the ring significantly influences its chemical properties and reactivity. The chlorine atom, being an electronegative substituent, can enhance the compound's electrophilic character, while the methoxy groups contribute to its overall electron-donating ability, affecting its solubility and interaction with other molecules. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its structure allows for potential applications in agrochemicals or as intermediates in organic synthesis. The compound is typically stable under standard conditions but may undergo reactions such as nucleophilic substitution or electrophilic aromatic substitution depending on the reaction environment. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

4-Chloro-3,5-dimethoxypyridazine

<p>4-Chloro-3,5-dimethoxypyridazine is a tautomeric compound that has been synthesized and characterized. The form of the molecule depends on the pH. At low pH, it exists in the form of an ion with a negative charge. When neutralized, it exists as a protonated molecule and at high pH, it exists as an ion with a positive charge. 4-Chloro-3,5-dimethoxypyridazine has been used to synthesise analogues with improved properties.</p>

CAS 63910-48-5

4-chloro-3,5-dimethoxypyridazine

4-Chloro-3,5-dimethoxypyridazine

Ref: IN-DA0036YZ

4-Chloro-3,5-dimethoxypyridazine

Ref: 10-F324502

4-Chloro-3,5-dimethoxypyridazine

Ref: 3D-NCA91048