Understanding the Properties and Applications of 4-(Trifluoromethyl)benzoyl Chloride
4-(Trifluoromethyl)benzoyl Chloride, identified by its CAS number 329-15-7, is a highly reactive organic compound with significant utility across various chemical sectors. Its molecular structure, featuring both a benzoyl chloride functional group and a potent trifluoromethyl substituent, makes it a valuable intermediate for a wide array of synthetic transformations. For professionals looking to buy 4-(Trifluoromethyl)benzoyl Chloride, understanding its properties is key to leveraging its full potential.
Physically, this compound is typically encountered as a liquid. Its chemical reactivity stems from the electrophilic nature of the carbonyl carbon in the benzoyl chloride moiety, making it an excellent acylating agent. The trifluoromethyl group (-CF3) significantly influences the compound's electronic properties and the reactivity of the benzoyl chloride group, often enhancing the lipophilicity and metabolic stability of molecules into which it is incorporated. This makes it particularly attractive for applications in pharmaceuticals and agrochemicals.
In terms of applications, 4-(Trifluoromethyl)benzoyl Chloride serves as a crucial building block for fluorinated organic compounds. Its use is prevalent in the synthesis of APIs, where it can contribute to improved drug efficacy and pharmacokinetic profiles. It also finds application in the agrochemical industry for developing novel pesticides and herbicides. Furthermore, its potential extends to materials science, where it can be used to modify polymers or create specialty materials with enhanced properties.
When sourcing this chemical, prospective buyers often search for a reliable manufacturer who can provide consistent quality and volume. Many turn to established chemical production hubs, such as China, to secure competitive pricing. It is advisable for buyers to obtain detailed technical specifications and purity data (e.g., ≥97%) from their chosen supplier. Understanding the optimal storage conditions and safety precautions, as outlined in the Safety Data Sheet (SDS), is also essential for safe and effective use.
Perspectives & Insights
Nano Explorer 01
“For professionals looking to buy 4-(Trifluoromethyl)benzoyl Chloride, understanding its properties is key to leveraging its full potential.”
Data Catalyst One
“Its chemical reactivity stems from the electrophilic nature of the carbonyl carbon in the benzoyl chloride moiety, making it an excellent acylating agent.”
Chem Thinker Labs
“The trifluoromethyl group (-CF3) significantly influences the compound's electronic properties and the reactivity of the benzoyl chloride group, often enhancing the lipophilicity and metabolic stability of molecules into which it is incorporated.”