3-Morpholin-4-yl-5-(trifluoromethyl)benzonitrile is a chemical compound characterized by its unique structural features, which include a morpholine ring and a trifluoromethyl group attached to a benzonitrile moiety. The presence of the morpholine ring contributes to its potential as a pharmacophore in medicinal chemistry, often enhancing solubility and bioavailability. The trifluoromethyl group is known for its electron-withdrawing properties, which can influence the compound's reactivity and interaction with biological targets. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with specific biological activities. Additionally, the presence of the nitrile functional group may impart unique chemical reactivity, making it a candidate for further chemical modifications. As with many fluorinated compounds, it is essential to handle this substance with care due to potential environmental and health impacts associated with fluorinated chemicals.

3-morpholin-4-yl-5-(trifluoromethyl)benzonitrile

220954-14-3: 3-Morpholin-4-yl-5-(trifluoromethyl)benzonitrile is a chemical compound characterized by its unique structural features, which include a morpholine ring and a trifluoromethyl group attached to a benzonitrile moiety. The presence of the morpholine ring contributes to its potential as a pharmacophore in medicinal chemistry, often enhancing solubility and bioavailability. The trifluoromethyl group is known for its electron-withdrawing properties, which can influence the compound's reactivity and interaction with biological targets. This compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with specific biological activities. Additionally, the presence of the nitrile functional group may impart unique chemical reactivity, making it a candidate for further chemical modifications. As with many fluorinated compounds, it is essential to handle this substance with care due to potential environmental and health impacts associated with fluorinated chemicals.

CAS 220954-14-3

3-morpholin-4-yl-5-(trifluoromethyl)benzonitrile

3-Morpholino-5-(trifluoromethyl)benzonitrile

Ref: IN-DA00CGB8

3-(Morpholin-4-yl)-5-(trifluoromethyl)benzonitrile

Ref: 54-PC200405

3-Morpholino-5-(trifluoromethyl)benzonitrile

Ref: 10-F316775