2-(5,7-Difluoro-2-methyl-1H-indol-3-yl)ethanamine, with the CAS number 383145-87-7, is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features two fluorine atoms at the 5 and 7 positions of the indole ring, contributing to its unique electronic properties and potential biological activity. The presence of a methyl group at the 2 position and an ethanamine side chain enhances its solubility and reactivity. Such modifications can influence the compound's interactions with biological targets, making it of interest in medicinal chemistry and drug development. The compound may exhibit various pharmacological properties, potentially acting as a ligand for specific receptors or enzymes. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its stability, solubility, and reactivity would be assessed through various analytical methods. Overall, this compound represents a class of indole derivatives that may have significant implications in pharmaceutical research.

2-(5,7-difluoro-2-methyl-1H-indol-3-yl)ethanamine

383145-87-7: 2-(5,7-Difluoro-2-methyl-1H-indol-3-yl)ethanamine, with the CAS number 383145-87-7, is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features two fluorine atoms at the 5 and 7 positions of the indole ring, contributing to its unique electronic properties and potential biological activity. The presence of a methyl group at the 2 position and an ethanamine side chain enhances its solubility and reactivity. Such modifications can influence the compound's interactions with biological targets, making it of interest in medicinal chemistry and drug development. The compound may exhibit various pharmacological properties, potentially acting as a ligand for specific receptors or enzymes. Its synthesis and characterization would typically involve standard organic chemistry techniques, and its stability, solubility, and reactivity would be assessed through various analytical methods. Overall, this compound represents a class of indole derivatives that may have significant implications in pharmaceutical research.

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CAS 383145-87-7

2-(5,7-difluoro-2-methyl-1H-indol-3-yl)ethanamine

2-(5,7-Difluoro-2-Methyl-1H-Indol-3-Yl)Ethanamine

Ref: 3D-FD91643