(2,4,5-Trifluoro-3-methoxy-phenyl)methanamine, with the CAS number 886362-79-4, is a chemical compound characterized by its unique structure, which includes a phenyl ring substituted with three fluorine atoms and a methoxy group, along with a methanamine functional group. The presence of trifluoromethyl groups typically enhances the compound's lipophilicity and can influence its biological activity, making it of interest in pharmaceutical research. The methoxy group contributes to the compound's electron-donating properties, potentially affecting its reactivity and interaction with biological targets. This compound may exhibit interesting properties such as increased stability and altered solubility compared to its non-fluorinated counterparts. Additionally, the presence of the amine group suggests potential for hydrogen bonding, which can play a significant role in its interactions with other molecules. Overall, this compound's unique combination of functional groups positions it as a candidate for various applications, particularly in medicinal chemistry and material science.

(2,4,5-trifluoro-3-methoxy-phenyl)methanamine

886362-79-4: (2,4,5-Trifluoro-3-methoxy-phenyl)methanamine, with the CAS number 886362-79-4, is a chemical compound characterized by its unique structure, which includes a phenyl ring substituted with three fluorine atoms and a methoxy group, along with a methanamine functional group. The presence of trifluoromethyl groups typically enhances the compound's lipophilicity and can influence its biological activity, making it of interest in pharmaceutical research. The methoxy group contributes to the compound's electron-donating properties, potentially affecting its reactivity and interaction with biological targets. This compound may exhibit interesting properties such as increased stability and altered solubility compared to its non-fluorinated counterparts. Additionally, the presence of the amine group suggests potential for hydrogen bonding, which can play a significant role in its interactions with other molecules. Overall, this compound's unique combination of functional groups positions it as a candidate for various applications, particularly in medicinal chemistry and material science.

CAS 886362-79-4

(2,4,5-trifluoro-3-methoxy-phenyl)methanamine

3-Methoxy-2,4,5-trifluorobenzylamine

Ref: IN-DA0049MC

3-Methoxy-2,4,5-trifluorobenzylamine

Ref: 54-PC911358

2,4,5-Trifluoro-3-methoxybenzylamine

Ref: 10-F040439