Benzeneacetonitrile, α-hydroxy-4-(trifluoromethyl)-, also known by its CAS number 168013-75-0, is an organic compound characterized by its unique functional groups. It features a benzene ring substituted with a trifluoromethyl group and an α-hydroxy group adjacent to a nitrile group. This structure imparts distinct chemical properties, including polarity and reactivity. The presence of the trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity, making it of interest in pharmaceutical and agrochemical research. The α-hydroxy group contributes to its potential as a chiral building block in synthesis. Additionally, the nitrile functional group can participate in various chemical reactions, such as nucleophilic additions and hydrolysis. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. Its applications may extend to the development of intermediates in organic synthesis, particularly in the creation of more complex molecules in medicinal chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

Benzeneacetonitrile, a-hydroxy-4-(trifluoromethyl)-

168013-75-0: Benzeneacetonitrile, α-hydroxy-4-(trifluoromethyl)-, also known by its CAS number 168013-75-0, is an organic compound characterized by its unique functional groups. It features a benzene ring substituted with a trifluoromethyl group and an α-hydroxy group adjacent to a nitrile group. This structure imparts distinct chemical properties, including polarity and reactivity. The presence of the trifluoromethyl group enhances the compound's lipophilicity and can influence its biological activity, making it of interest in pharmaceutical and agrochemical research. The α-hydroxy group contributes to its potential as a chiral building block in synthesis. Additionally, the nitrile functional group can participate in various chemical reactions, such as nucleophilic additions and hydrolysis. The compound is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. Its applications may extend to the development of intermediates in organic synthesis, particularly in the creation of more complex molecules in medicinal chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.

Benzeneacetonitrile, .α.-hydroxy-4-(trifluoromethyl)-

2-Hydroxy-2-[4-(trifluoromethyl)phenyl]acetonitrile

CAS 168013-75-0

Benzeneacetonitrile, a-hydroxy-4-(trifluoromethyl)-

Benzeneacetonitrile, .α.-hydroxy-4-(trifluoromethyl)-

Ref: IN-DA007VOF

2-Hydroxy-2-[4-(trifluoromethyl)phenyl]acetonitrile

Ref: 54-PC101375

2-Hydroxy-2-[4-(trifluoromethyl)phenyl]acetonitrile

Ref: 10-F546378