Benzenemethanamine, α-methyl-4-(trifluoromethoxy)-, (αS)-, with the CAS number 951247-75-9, is a chiral organic compound characterized by its amine functional group and a trifluoromethoxy substituent. This compound features a benzene ring, which contributes to its aromatic properties, and an α-methyl group that influences its steric and electronic characteristics. The presence of the trifluoromethoxy group enhances its lipophilicity and may affect its reactivity and interaction with biological systems. As a chiral molecule, it exists in two enantiomeric forms, with the (αS)- designation indicating a specific spatial arrangement of its atoms. Such compounds are often of interest in medicinal chemistry due to their potential biological activity, including applications in drug development. The trifluoromethoxy group can also impart unique properties, such as increased metabolic stability or altered binding affinity to biological targets. Overall, this compound exemplifies the complexity and diversity of organic molecules used in various chemical and pharmaceutical applications.

Benzenemethanamine,a-methyl-4-(trifluoromethoxy)-, (aS)-

951247-75-9: Benzenemethanamine, α-methyl-4-(trifluoromethoxy)-, (αS)-, with the CAS number 951247-75-9, is a chiral organic compound characterized by its amine functional group and a trifluoromethoxy substituent. This compound features a benzene ring, which contributes to its aromatic properties, and an α-methyl group that influences its steric and electronic characteristics. The presence of the trifluoromethoxy group enhances its lipophilicity and may affect its reactivity and interaction with biological systems. As a chiral molecule, it exists in two enantiomeric forms, with the (αS)- designation indicating a specific spatial arrangement of its atoms. Such compounds are often of interest in medicinal chemistry due to their potential biological activity, including applications in drug development. The trifluoromethoxy group can also impart unique properties, such as increased metabolic stability or altered binding affinity to biological targets. Overall, this compound exemplifies the complexity and diversity of organic molecules used in various chemical and pharmaceutical applications.

(S)-1-(4-(Trifluoromethoxy)phenyl)ethanamine

(1S)-1-[4-(Trifluoromethoxy)phenyl]ethylamine

CAS 951247-75-9

Benzenemethanamine,a-methyl-4-(trifluoromethoxy)-, (aS)-

(S)-1-(4-(Trifluoromethoxy)phenyl)ethanamine

Ref: IN-DA005T64

(1S)-1-[4-(Trifluoromethoxy)phenyl]ethylamine

Ref: 54-PC7515

(S)-1-(4-(Trifluoromethoxy)phenyl)ethanamine

Ref: 10-F222661