The Chemistry of Methallyl Chloride (CAS 563-47-3): Properties and Synthesis Pathways
Methallyl chloride, known by its CAS number 563-47-3, is a fascinating organochlorine compound whose chemical characteristics underpin its wide range of industrial applications. Understanding its properties and synthesis pathways is fundamental to appreciating its role as a key intermediate in various chemical manufacturing processes.
Chemically, Methallyl chloride has the molecular formula C4H7Cl, with a molecular weight of approximately 90.55 g/mol. It is typically described as a colorless liquid that possesses a pungent odor, characteristic of many chlorinated hydrocarbons. Its molecular structure features a double bond and a chlorine atom attached to a methyl-substituted allyl group. This structural arrangement imbues Methallyl chloride with significant reactivity, particularly due to the presence of the allylic chloride functionality.
The reactivity of Methallyl chloride is a defining feature. The chlorine atom is relatively labile, making it susceptible to nucleophilic substitution reactions. This property allows it to act as an effective alkylating agent, enabling the introduction of the methallyl group into other molecules. Furthermore, the double bond can undergo addition reactions and polymerization, which are critical for its use in creating polymers and other complex organic structures. Its involvement in reactions like Grignard reactions or as a precursor in Wittig reactions further showcases its versatility in organic synthesis.
The synthesis of Methallyl chloride typically involves the chlorination of isobutylene or related precursors. One common method involves the high-temperature chlorination of isobutylene, where specific reaction conditions are controlled to favor the formation of Methallyl chloride over other chlorinated products. Alternative routes might involve the dehydrochlorination of dichlorinated compounds or other halogenation and elimination sequences. The efficiency and selectivity of these synthesis pathways are crucial for producing Methallyl chloride at an industrial scale with the required purity.
For manufacturers and researchers working with Methallyl chloride, understanding these chemical properties and synthesis routes is essential for optimizing reaction yields, ensuring product quality, and maintaining safety standards. Companies like NINGBO INNO PHARMCHEM CO.,LTD. focus on providing high-purity Methallyl chloride, often produced through optimized synthesis pathways, to meet the stringent requirements of industries such as pharmaceuticals and agrochemicals. The chemical versatility of Methallyl chloride ensures its continued importance in the field of synthetic chemistry.
Perspectives & Insights
Data Seeker X
“This structural arrangement imbues Methallyl chloride with significant reactivity, particularly due to the presence of the allylic chloride functionality.”
Chem Reader AI
“The chlorine atom is relatively labile, making it susceptible to nucleophilic substitution reactions.”
Agile Vision 2025
“This property allows it to act as an effective alkylating agent, enabling the introduction of the methallyl group into other molecules.”