This article provides a comprehensive overview of 2,4,6-Trimethylbenzoyl Chloride (CAS 938-18-1), a chemical compound widely used in research. It covers its physical and chemical properties, synthesis methods, applications in various fields, safety considerations, and storage guidelines. By understanding these aspects, researchers can effectively utilize this compound in their experiments and ensure safe handling.<\/p>\n
2,4,6-Trimethylbenzoyl Chloride, also known as trimethylbenzoyl chloride, is a colorless to pale yellow liquid with a pungent odor. It is a derivative of benzoic acid, where the hydroxyl group is replaced by a chlorine atom. This compound is widely used in organic synthesis due to its versatile reactivity and ease of handling. In this article, we will delve into the essential information that researchers need to know about 2<\/a>,4,6-Trimethylbenzoyl Chloride for their research endeavors.<\/p>\n 2,4,6-Trimethylbenzoyl Chloride has a molecular formula of C8<\/sub>H9<\/sub>ClO and a molecular weight of 157.59 g\/mol. It is soluble in organic solvents such as chloroform, acetone, and ether but is not soluble in water. The compound has a melting point of -16\u00b0C to -18\u00b0C and a boiling point of 244\u00b0C to 246\u00b0C. It is also highly reactive and can undergo various chemical transformations, including nucleophilic substitution, addition, and elimination reactions.<\/p>\n The synthesis of 2,4,6-Trimethylbenzoyl Chloride can be achieved through several methods, including the reaction of 2,4,6-trimethylbenzoic acid with thionyl chloride or phosphorus pentachloride. Another common method involves the reaction of 2,4,6-trimethylbenzoic anhydride with hydrogen chloride. These synthetic routes provide researchers with flexibility in choosing the most suitable method based on their specific requirements and available resources.<\/p>\nPropiedades f\u00edsicas y qu\u00edmicas<\/h3>\n
M\u00e9todos de s\u00edntesis<\/h3>\n
Aplicaciones en s\u00edntesis org\u00e1nica<\/h3>\n