2,2,2-Trifluoro-1-(1H-indol-3-yl)ethanamine, commonly referred to as a racemic mixture, is a chemical compound characterized by its unique structure that includes a trifluoroethyl group and an indole moiety. The presence of three fluorine atoms contributes to its lipophilicity and potential biological activity, making it of interest in medicinal chemistry. The indole ring, a common structural motif in many biologically active compounds, may influence its interaction with various biological targets, including receptors and enzymes. As a racemic mixture, it contains equal amounts of two enantiomers, which can exhibit different pharmacological properties. This compound is typically studied for its potential applications in drug development, particularly in the fields of neuroscience and psychiatry, due to its structural similarity to neurotransmitters. Safety and handling precautions are essential, as with many fluorinated compounds, due to their potential toxicity and environmental impact. Overall, 2,2,2-trifluoro-1-(1H-indol-3-yl)ethanamine represents a fascinating subject for further research in chemical and pharmaceutical sciences.

2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)ETHANAMINE (racemic)

126954-11-8: 2,2,2-Trifluoro-1-(1H-indol-3-yl)ethanamine, commonly referred to as a racemic mixture, is a chemical compound characterized by its unique structure that includes a trifluoroethyl group and an indole moiety. The presence of three fluorine atoms contributes to its lipophilicity and potential biological activity, making it of interest in medicinal chemistry. The indole ring, a common structural motif in many biologically active compounds, may influence its interaction with various biological targets, including receptors and enzymes. As a racemic mixture, it contains equal amounts of two enantiomers, which can exhibit different pharmacological properties. This compound is typically studied for its potential applications in drug development, particularly in the fields of neuroscience and psychiatry, due to its structural similarity to neurotransmitters. Safety and handling precautions are essential, as with many fluorinated compounds, due to their potential toxicity and environmental impact. Overall, 2,2,2-trifluoro-1-(1H-indol-3-yl)ethanamine represents a fascinating subject for further research in chemical and pharmaceutical sciences.

2,2,2-Trifluoro-1-(1H-indol-3-yl)ethanamine

CAS 126954-11-8

2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)ETHANAMINE (racemic)

2,2,2-Trifluoro-1-(1H-indol-3-yl)ethanamine

Ref: 54-PC1006873

2,2,2-Trifluoro-1-(1H-indol-3-yl)ethan-1-amine

Ref: 3D-BFA95411