3-Chloro-4-methylpyridazine is a heterocyclic organic compound characterized by a pyridazine ring, which is a six-membered aromatic ring containing two nitrogen atoms at adjacent positions. The presence of a chlorine atom at the 3-position and a methyl group at the 4-position contributes to its unique chemical properties. This compound typically appears as a colorless to light yellow liquid or solid, depending on its physical state at room temperature. It is known for its potential applications in pharmaceuticals and agrochemicals due to its reactivity and ability to participate in various chemical reactions, such as nucleophilic substitutions and electrophilic aromatic substitutions. The compound's molecular structure influences its solubility, stability, and reactivity, making it of interest in synthetic organic chemistry. Safety data should be consulted for handling and storage, as halogenated compounds can exhibit toxicity and environmental concerns. Overall, 3-Chloro-4-methylpyridazine is a valuable compound in chemical research and development.

3-Chloro-4-methylpyridazine

68206-04-2: Pyridazine, 3-Chloro-4-Methyl-

3-Chloro-4-methylpyridazine is an oxychloride byproduct that has been found to have antiviral activity. It is a research chemical and industrial chemical that has been used in the preparation of 3-chloro-4-methylpyridine, which is used in the production of phosphorus oxychloride. 3-Chloro-4-methylpyridazine can be obtained by reacting with hydrochloric acid or sodium hydroxide solution with phosphorus oxychloride. This process yields a mixture of 3-chloro-4-methylpyridine and 4,5,6,7,8,9,10 (octahydro) pyrimido[1,2:3,-a]azepin. The product yield from this reaction can be improved by adding sodium bicarbonate and palladium.

CAS 68206-04-2: 3-Chloro-4-methylpyridazine

3-Chloro-4-methylpyridazine

Ref: 10-F067467

3-Chloro-4-methylpyridazine

Ref: IN-DA005LX0

3-Chloro-4-methylpyridazine

Ref: 3D-FC151278

3-Chloro-4-methylpyridazine

Ref: 54-OR42178