2,2-Dimethyl-N-[2-methyl-3-(trifluoromethyl)phenyl]-propionamide, identified by its CAS number 150783-50-9, is a synthetic organic compound characterized by its amide functional group. This compound features a propionamide backbone, which is substituted with a dimethyl group and a phenyl ring that carries a trifluoromethyl group. The presence of the trifluoromethyl group enhances the compound's lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. The compound is likely to exhibit moderate to high stability under standard conditions, although specific reactivity can depend on the surrounding environment and conditions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of compounds with specific biological targets. Additionally, the presence of fluorine atoms can impart unique electronic properties, which may affect the compound's interaction with biological systems. Safety and handling precautions should be observed, as with all chemical substances, particularly those with fluorinated groups, due to potential toxicity and environmental impact.

2,2-DIMETHYL-N-[2-METHYL-3-(TRIFLUOROMETHYL)PHENYL]-PROPIONAMIDE

150783-50-9: 2,2-Dimethyl-N-[2-methyl-3-(trifluoromethyl)phenyl]-propionamide, identified by its CAS number 150783-50-9, is a synthetic organic compound characterized by its amide functional group. This compound features a propionamide backbone, which is substituted with a dimethyl group and a phenyl ring that carries a trifluoromethyl group. The presence of the trifluoromethyl group enhances the compound's lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. The compound is likely to exhibit moderate to high stability under standard conditions, although specific reactivity can depend on the surrounding environment and conditions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of compounds with specific biological targets. Additionally, the presence of fluorine atoms can impart unique electronic properties, which may affect the compound's interaction with biological systems. Safety and handling precautions should be observed, as with all chemical substances, particularly those with fluorinated groups, due to potential toxicity and environmental impact.

<p>Applications An intermediate for the preparation of Flunixin and other derivatives of this analgesic.<br></p>

CAS 150783-50-9

2,2-DIMETHYL-N-[2-METHYL-3-(TRIFLUOROMETHYL)PHENYL]-PROPIONAMIDE

2-Methyl-3-(trifluoromethyl)pivalanilide

Ref: TR-M330925