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1,3-Difluoroacetone CAS:453-14-5

1,3-Difluoroacetone is a significant chemical compound renowned for its unique molecular structure and diverse applications across various industries. With the chemical formula C3H4F2O, it is characterized by the presence of two fluorine atoms attached to a ketone functional group. This compound is synthesized through the fluorination of acetone, resulting in a volatile liquid with distinctive chemical properties. 1,3-Difluoroacetone is valued for its role as a precursor in organic synthesis and its potential applications in pharmaceuticals, agrochemicals, and materials science due to its reactive nature and specific molecular attributes.


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Application and Effect:

1,3-Difluoroacetone (DFA) is a versatile compound with unique chemical properties that make it valuable in various industrial applications. Properties 1,3-Difluoroacetone is characterized by its molecular structure, which includes a ketone group (-C(=O)-) substituted with two fluorine atoms. This structural feature imparts notable reactivity and stability to the compound, influencing its applications in organic synthesis and chemical reactions. DFA typically exists as a volatile liquid with a boiling point around 80°C and exhibits moderate solubility in polar solvents like water and acetone. Its chemical stability under mild conditions makes it suitable for use as a building block in the synthesis of complex organic molecules. Uses Organic Synthesis: One of the primary applications of 1,3-difluoroacetone lies in organic synthesis, where it serves as a key intermediate or precursor. Its reactive ketone group allows for the introduction of fluorine atoms into organic molecules, facilitating the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals with desired fluorinated functionalities. Chemical Reagent: DFA is utilized as a chemical reagent in various laboratory and industrial processes, including the modification of biomolecules and the production of fluorinated compounds. Its ability to undergo nucleophilic substitution and condensation reactions broadens its utility in diverse chemical transformations. Materials Science: In materials science, DFA finds applications in the development of specialty materials and coatings. Its reactivity and ability to influence surface properties make it suitable for modifying material surfaces to enhance durability, chemical resistance, and performance under specific environmental conditions. Synthesis 1,3-Difluoroacetone can be synthesized by fluorinating acetone under controlled conditions using fluorinating agents such as hydrogen fluoride (HF) or elemental fluorine (F2). The fluorination process replaces hydrogen atoms in acetone with fluorine atoms, yielding 1,3-difluoroacetone as the main product. Purification methods typically involve distillation or solvent extraction to obtain DFA in high purity suitable for industrial and laboratory applications. In summary, 1,3-difluoroacetone is a versatile compound with significant applications in organic synthesis, chemical reactivity, and materials science. Its unique properties as a fluorinated ketone enable diverse functionalities, supporting advancements in various industrial sectors and contributing to the development of specialized chemicals and materials.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C3H4F2O
Assay 99%
Appearance white powder
CAS No.  453-14-5
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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