3,3-Difluorobutan-1-ol is an organic compound characterized by the presence of a hydroxyl group (-OH) attached to a butane backbone, specifically at the first carbon position, along with two fluorine atoms substituted at the third carbon. This structure imparts unique properties to the molecule, including increased polarity due to the hydroxyl group, which enhances its solubility in polar solvents. The fluorine atoms contribute to the compound's reactivity and can influence its boiling and melting points compared to its non-fluorinated counterparts. As a secondary alcohol, it can participate in various chemical reactions, such as oxidation and substitution. The presence of fluorine also suggests potential applications in pharmaceuticals and agrochemicals, where fluorinated compounds often exhibit improved biological activity and stability. Additionally, 3,3-difluorobutan-1-ol's molecular structure may lead to interesting interactions in biological systems, making it a compound of interest in medicinal chemistry and materials science. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity and reactivity.

3,3-difluorobutan-1-ol

858359-36-1: 3,3-Difluorobutan-1-ol is an organic compound characterized by the presence of a hydroxyl group (-OH) attached to a butane backbone, specifically at the first carbon position, along with two fluorine atoms substituted at the third carbon. This structure imparts unique properties to the molecule, including increased polarity due to the hydroxyl group, which enhances its solubility in polar solvents. The fluorine atoms contribute to the compound's reactivity and can influence its boiling and melting points compared to its non-fluorinated counterparts. As a secondary alcohol, it can participate in various chemical reactions, such as oxidation and substitution. The presence of fluorine also suggests potential applications in pharmaceuticals and agrochemicals, where fluorinated compounds often exhibit improved biological activity and stability. Additionally, 3,3-difluorobutan-1-ol's molecular structure may lead to interesting interactions in biological systems, making it a compound of interest in medicinal chemistry and materials science. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity and reactivity.

CAS 858359-36-1

3,3-difluorobutan-1-ol

3,3-Difluorobutan-1-ol

Ref: 54-PC49818

3,3-Difluorobutan-1-ol

Ref: 10-F101918

3,3-Difluorobutan-1-ol

Ref: TR-D455900

3,3-Difluorobutan-1-ol

Ref: 3D-IJB35936