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2-Ethoxyethyl chloroformate CAS:628-64-8

2-Ethoxyethyl chloroformate is an organic compound comprising a chloroformate functional group attached to a 2-ethoxyethyl moiety. This reagent functions as a powerful acylating agent in organic synthesis, facilitating the formation of esters and carbamates through reactions with nucleophiles such as alcohols and amines. The ethoxy substituent enhances the solubility and reactivity of the resultant compounds, making them suitable for various applications in pharmaceuticals, agrochemicals, and polymer chemistry. Understanding the properties and reactivity of 2-ethoxyethyl chloroformate is essential for chemists aiming to utilize this compound effectively in diverse synthetic strategies.


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Application and Effect:

2-Ethoxyethyl chloroformate (C10H13ClO3) is a valuable chemical reagent widely used in organic synthesis due to its versatility as an acylating agent. With a structure comprising an ethoxy group linked to a chloroformate functional group, it facilitates efficient nucleophilic acyl substitution reactions. This characteristic makes 2-ethoxyethyl chloroformate particularly effective in synthesizing esters and carbamates when reacted with various nucleophiles, including alcohols and amines. One of the primary applications of 2-ethoxyethyl chloroformate is in the formation of esters. When combined with alcohols, it produces ethoxyethyl esters that exhibit enhanced stability and desirable physicochemical properties. These esters find use in a variety of industries, including pharmaceuticals, cosmetics, and food processing, where they can act as flavoring agents, solvents, or emulsifiers. In addition to ester synthesis, 2-ethoxyethyl chloroformate plays a crucial role in producing carbamates, which are important intermediates in drug development and agricultural chemicals. The incorporation of the ethoxy group can improve the biological activity and selectivity of these compounds, enhancing their therapeutic potential. Furthermore, 2-ethoxyethyl chloroformate serves as a protecting group for alcohols and amines during multi-step organic syntheses. By temporarily modifying reactive sites, it allows chemists to control reaction pathways more effectively, enabling selective transformations while minimizing unwanted side reactions. The mild conditions required for the removal of the protecting group make it an attractive choice in complex synthetic routes. Despite its numerous advantages, safe handling of 2-ethoxyethyl chloroformate is necessary due to its potential irritant effects and toxicity. Chemists must observe appropriate safety measures, including using personal protective equipment and working in well-ventilated areas. In summary, 2-ethoxyethyl chloroformate is an essential reagent in organic chemistry, aiding in the synthesis of complex molecules across pharmaceuticals, agrochemicals, and materials science. Its exceptional reactivity and versatility continue to make it invaluable in modern chemical research and development.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C5H9ClO3
Assay 99%
Appearance white powder
CAS No.  628-64-8
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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