Ethyl 2,2-Difluorohexanoate is an organic compound characterized by its ester functional group, which is formed from the reaction of hexanoic acid and ethanol, with the addition of two fluorine atoms at the second carbon of the hexanoate chain. This compound typically appears as a colorless liquid with a fruity odor, which is common among esters. Its molecular formula reflects the presence of carbon, hydrogen, and fluorine atoms, contributing to its unique properties. Ethyl 2,2-Difluorohexanoate is known for its relatively low boiling point and moderate solubility in organic solvents, while being less soluble in water due to its hydrophobic hydrocarbon chain. The presence of fluorine atoms can enhance its chemical stability and influence its reactivity, making it of interest in various applications, including as a potential intermediate in organic synthesis and in the development of pharmaceuticals. Safety data should be consulted for handling and exposure guidelines, as fluorinated compounds can exhibit specific toxicological profiles.

Ethyl 2,2-Difluorohexanoate

74106-81-3: Hexanoic acid, 2,2-difluoro-, ethyl ester

Ethyl 2,2-difluorohexanoate is a stable, non-volatile liquid that is soluble in many organic solvents. It can be synthesized by the reaction of ethyl formate and hydrogen fluoride in acetonitrile with a palladium catalyst. This compound has been shown to be an excellent reagent for the synthesis of sulfoxides and sulfones. Ethyl 2,2-difluorohexanoate has been used as a catalyst in industrial processes such as the production of polyester resins and nylon fibers. It is also used as a solvent in analytical chemistry procedures such as gas chromatography and high performance liquid chromatography.

CAS 74106-81-3: Ethyl 2,2-Difluorohexanoate

Ethyl 2,2-difluorohexanoate

Ref: 3D-FE97767

Ethyl 2,2-difluorohexanoate

Ref: 54-PC48304

Ethyl 2,2-difluorohexanoate

Ref: IN-DA005TT6

Ethyl-2,2-difluorohexanoate

Ref: 10-F035963