2,2-difluoroacetamide CAS: 359-38-6
Catalog Number | XD93584 |
Product Name | 2,2-difluoroacetamide |
CAS | 359-38-6 |
Molecular Formula | C2H3F2NO |
Molecular Weight | 95.05 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2,2-difluoroacetamide, also known as DFA, is a chemical compound with the molecular formula C2H3F2NO. It is a colorless, odorless crystalline solid that is soluble in polar solvents like water and methanol. 2,2-difluoroacetamide has various applications in different fields due to its unique properties.One of the primary uses of 2,2-difluoroacetamide is as a building block in organic synthesis. It can undergo various chemical reactions to form a wide range of compounds. For example, it can be used as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Through appropriate modifications and functional group transformations, 2,2-difluoroacetamide can be incorporated into complex molecules, imparting desired properties and functionalities.Furthermore, 2,2-difluoroacetamide is widely used as a reagent in the synthesis of fluorinated compounds. Fluorinated organic molecules often exhibit unique properties like increased lipophilicity, enhanced stability, and altered pharmacokinetics. By utilizing 2,2-difluoroacetamide as a starting material, chemists can introduce fluorine atoms into desired positions within a molecule, resulting in novel compounds with improved characteristics.Another notable application of 2,2-difluoroacetamide is its role as a protective group in organic synthesis. It can be used to temporarily protect certain functional groups during chemical reactions. The presence of the 2,2-difluoroacetamide group shields the protected functional group from unwanted side reactions, allowing specific transformations to occur selectively. After the desired reactions have taken place, the 2,2-difluoroacetamide group can be easily removed, restoring the original functionality.In addition to its uses in organic synthesis, 2,2-difluoroacetamide finds applications in the field of analytical chemistry. It can be used as a derivatizing agent to enhance the detection and analysis of various compounds. By reacting with certain functional groups or compounds of interest, such as amines or thiols, 2,2-difluoroacetamide can facilitate their identification and quantification by gas chromatography, liquid chromatography, or mass spectrometry.In summary, 2,2-difluoroacetamide is a versatile compound with various applications in organic synthesis and analytical chemistry. Its role as a building block in the synthesis of pharmaceuticals and agrochemicals, its use as a protective group, and its utility as a derivatizing agent highlight its importance in different fields. The ability to introduce fluorine atoms into molecules through 2,2-difluoroacetamide provides access to a wide range of fluorinated compounds with unique properties. Overall, the use of 2,2-difluoroacetamide contributes to the development of new materials and compounds with improved characteristics and performance.