3-(4-Trifluoromethyl-phenyl)-propionaldehyde, with the CAS number 166947-09-7, is an organic compound characterized by its aldehyde functional group and a trifluoromethyl substituent on a phenyl ring. This compound typically exhibits a clear to pale yellow liquid appearance and has a distinctive aromatic odor. The presence of the trifluoromethyl group enhances its lipophilicity and can influence its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The aldehyde functional group is reactive, allowing for various chemical transformations, including condensation and oxidation reactions. Additionally, the compound's molecular structure contributes to its potential applications in materials science and as a building block in the synthesis of more complex molecules. Safety data indicates that, like many aldehydes, it should be handled with care due to potential irritant properties and the need for proper ventilation during use.

3-(4-TRIFLUOROMETHYL-PHENYL)-PROPIONALDEHYDE

166947-09-7: 3-[4-(Trifluoromethyl)phenyl]propanal

3-(4-Trifluoromethylphenyl)propanal

Benzenepropanal, 4-(trifluoromethyl)-

3-(4-(Trifluoromethyl)phenyl)propanal

CAS 166947-09-7: 3-(4-TRIFLUOROMETHYL-PHENYL)-PROPIONALDEHYDE

3-(4-Trifluoromethylphenyl)propanal

Ref: TR-T791105

Benzenepropanal, 4-(trifluoromethyl)-

Ref: IN-DA001X16

3-(4-(Trifluoromethyl)phenyl)propanal

Ref: 10-F787732

Cinacalcet Impurity 24

Ref: 4Z-C-4034

3-[4-(Trifluoromethyl)phenyl]propanal

Ref: 54-PC4059

Cinacalcet Impurity 25

Ref: ST-EA-CP-C21056