7-(Trifluoromethyl)-5-quinolinamine, with the CAS number 321-71-1, is a chemical compound that belongs to the class of quinoline derivatives. This compound features a quinoline ring system, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring. The presence of a trifluoromethyl group (-CF3) at the 7-position of the quinoline enhances its lipophilicity and can influence its biological activity. The amino group (-NH2) at the 5-position contributes to its potential as a building block in medicinal chemistry, as amines are often involved in hydrogen bonding and can serve as sites for further functionalization. This compound may exhibit interesting pharmacological properties, making it a subject of research in drug development. Its physical properties, such as solubility and melting point, can vary based on the specific conditions and purity of the sample. Overall, 7-(Trifluoromethyl)-5-quinolinamine is notable for its structural features that may confer unique chemical reactivity and biological activity.

7-(Trifluoromethyl)-5-quinolinamine

321-71-1: Quinoline, 5-amino-7-(trifluoromethyl)-, 5-Quinolinamine, 7-(trifluoromethyl)-, 7-(Trifluoromethyl)-5-quinolinamine

7-(TRIFLUOROMETHYL)QUINOLIN-5-AMINE

7-(Trifluoromethyl)quinolin-5-amine is a quinoline derivative that inhibits the activity of tyrosine kinases, including c-MET. It has been shown to inhibit the activation of c-MET in tumour cells and therefore may be useful for cancer treatment. The modifications to 7-(trifluoromethyl)quinolin-5-amine have not been extensively studied, but it contains a n-linked framework that does not appear to be susceptible to modification by other molecules. This compound is multisubstituted with trifluoromethyl groups on the phenyl group and side chain of the quinoline ring.

CAS 321-71-1: 7-(Trifluoromethyl)-5-quinolinamine

7-(TRIFLUOROMETHYL)QUINOLIN-5-AMINE

Ref: 10-F332479

7-(trifluoromethyl)quinolin-5-amine

Ref: 3D-AAA32171

7-(trifluoromethyl)quinolin-5-amine

Ref: IN-DA00CMNJ