Methyl 2,2-difluoro-3-methoxypropanoate is an organic compound characterized by its ester functional group, which is derived from methanol and a difluorinated propanoic acid. This compound features two fluorine atoms attached to the second carbon of the propanoate chain, contributing to its unique chemical properties, such as increased lipophilicity and potential reactivity in various chemical reactions. The methoxy group (-OCH3) at the third carbon enhances its solubility in organic solvents and may influence its reactivity in nucleophilic substitution reactions. Methyl 2,2-difluoro-3-methoxypropanoate is typically a colorless liquid at room temperature, with a moderate boiling point and density that are characteristic of esters. Its fluorinated structure may impart specific biological activities, making it of interest in medicinal chemistry and agrochemical applications. Safety data should be consulted for handling, as fluorinated compounds can exhibit unique toxicological profiles. Overall, this compound exemplifies the interplay between structure and reactivity in organic chemistry.

methyl 2,2-difluoro-3-methoxypropanoate

99497-39-9: Propanoic acid, 2,2-difluoro-3-methoxy-, methyl ester, Methyl 2,2-difluoro-3-methoxypropanoate

CAS 99497-39-9: methyl 2,2-difluoro-3-methoxypropanoate

Methyl 2,2-difluoro-3-methoxypropionate

Ref: 3D-ZDA49739