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2-Ethoxybenzoyl chloride CAS:42926-52-3

2-Ethoxybenzoyl chloride is an aromatic acyl chloride derived from 2-ethoxybenzoic acid. With the molecular formula C9H9ClO2, it features a benzene ring substituted with an ethoxy group and an acyl chloride functional group. This compound is primarily used in organic synthesis as an important intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its reactive acyl chloride group facilitates nucleophilic substitution reactions, enabling the formation of esters, amides, and other derivatives. Due to its utility in synthesizing complex molecules, 2-ethoxybenzoyl chloride has gained attention in both academic research and industrial applications.


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Application and Effect:

2-Ethoxybenzoyl chloride is a valuable chemical compound characterized by its unique structure consisting of a benzene ring bearing an ethoxy group (-OCH2CH3) and an acyl chloride functional group (-COCl). This compound is utilized extensively in organic chemistry due to its highly reactive nature. The presence of the acyl chloride functional group makes it particularly useful in nucleophilic acyl substitution reactions, which are essential for forming new carbon-carbon and carbon-heteroatom bonds. One of the primary applications of 2-ethoxybenzoyl chloride lies in the synthesis of various pharmaceutical agents. By reacting with nucleophiles such as amines or alcohols, it enables the production of amides and esters, respectively. These derivatives often serve as key building blocks in the development of active pharmaceutical ingredients (APIs). Consequently, 2-ethoxybenzoyl chloride is an important intermediate in drug development processes, contributing to the creation of diverse therapeutic compounds. In addition to pharmaceuticals, this acyl chloride is also employed in the production of agrochemicals, where it can be used to synthesize herbicides, pesticides, and fungicides. The ability to introduce specific functional groups through acylation reactions allows chemists to design molecules with targeted biological activity, enhancing the efficacy of agricultural products. Moreover, 2-ethoxybenzoyl chloride plays a role in the synthesis of materials such as polymers and surfactants. Its reactivity can be harnessed in polymer chemistry, enabling the incorporation of ethoxybenzoyl units into larger macromolecular structures, thereby modifying their properties. While handling 2-ethoxybenzoyl chloride, safety precautions are essential due to its corrosive nature and potential health hazards. Proper laboratory practices and personal protective equipment should be employed to prevent exposure. Overall, 2-ethoxybenzoyl chloride serves as a crucial reagent in organic synthesis, demonstrating its significance in advancing chemical research and industrial applications.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C9H9ClO2
Assay 99%
Appearance white powder
CAS No.  42926-52-3
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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