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Ethyl2,2-difluoroacetoacetate CAS:2266-48-0

Ethyl 2,2-difluoroacetoacetate is a fluorinated organic compound utilized in various chemical reactions, particularly in the synthesis of pharmaceuticals and agrochemicals. Its molecular structure contains two fluorine atoms attached to the acetoacetate moiety, imparting distinctive reactivity and selectivity in reactions.


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Application and Effect:

Ethyl 2,2-difluoroacetoacetate finds extensive applications in organic synthesis, primarily due to its versatile reactivity and ability to introduce fluorine atoms into target molecules. One of its key applications lies in the synthesis of pharmaceutical compounds. Fluorinated organic molecules often exhibit enhanced bioavailability, metabolic stability, and selectivity in drug-target interactions, making ethyl 2,2-difluoroacetoacetate a valuable building block in medicinal chemistry. Additionally, this compound is employed in the preparation of agrochemicals, where fluorinated functional groups can confer desirable properties such as increased potency, improved resistance to metabolic degradation, and reduced environmental impact. By incorporating ethyl 2,2-difluoroacetoacetate into the synthesis of pesticides and herbicides, researchers can develop compounds with enhanced efficacy and reduced ecological footprint. Furthermore, ethyl 2,2-difluoroacetoacetate serves as a valuable intermediate in the synthesis of specialty chemicals, including fluorinated polymers, dyes, and materials with unique electronic properties. Its ability to introduce fluorine atoms at specific positions within organic molecules enables the creation of compounds with tailored properties for diverse applications in materials science and industrial chemistry. In organic synthesis, ethyl 2,2-difluoroacetoacetate participates in various transformations, such as nucleophilic addition, substitution, and condensation reactions. Its reactivity is modulated by the electron-withdrawing nature of the fluorine substituents, which can facilitate regioselective and stereoselective transformations, thereby enabling the efficient construction of complex molecular architectures. Moreover, the presence of fluorine atoms in ethyl 2,2-difluoroacetoacetate imparts unique physicochemical properties to the resulting compounds, including altered acidity/basicity, lipophilicity, and intermolecular interactions. These properties are exploited in the design and synthesis of molecules for specific applications, ranging from drug discovery to materials engineering. Overall, ethyl 2,2-difluoroacetoacetate represents a valuable tool in the toolkit of synthetic chemists, enabling the construction of diverse organic molecules with enhanced properties for applications in pharmaceuticals, agrochemicals, materials science, and beyond.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C6H8F2O4
Assay 99%
Appearance white powder
CAS No.  2266-48-0
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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