6-(Trifluoromethyl)-1H-indazole is a chemical compound characterized by its indazole core, which is a bicyclic structure consisting of a five-membered ring fused to a six-membered ring. The presence of a trifluoromethyl group (-CF3) at the 6-position significantly influences its chemical properties, enhancing its lipophilicity and potentially its biological activity. This compound is typically a solid at room temperature and may exhibit stability under standard conditions, although it can be sensitive to moisture and light. The trifluoromethyl group is known to impart unique electronic properties, making the compound of interest in various fields, including medicinal chemistry and materials science. Its CAS number, 954239-22-6, allows for precise identification in chemical databases. The compound may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the reactivity of the indazole framework. Overall, 6-(trifluoromethyl)-1H-indazole is a versatile compound with potential applications in drug development and synthetic chemistry.

6-(trifluoromethyl)-1H-indazole

954239-22-6: 6-(Trifluoromethyl)-1H-indazole is a chemical compound characterized by its indazole core, which is a bicyclic structure consisting of a five-membered ring fused to a six-membered ring. The presence of a trifluoromethyl group (-CF3) at the 6-position significantly influences its chemical properties, enhancing its lipophilicity and potentially its biological activity. This compound is typically a solid at room temperature and may exhibit stability under standard conditions, although it can be sensitive to moisture and light. The trifluoromethyl group is known to impart unique electronic properties, making the compound of interest in various fields, including medicinal chemistry and materials science. Its CAS number, 954239-22-6, allows for precise identification in chemical databases. The compound may also participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the reactivity of the indazole framework. Overall, 6-(trifluoromethyl)-1H-indazole is a versatile compound with potential applications in drug development and synthetic chemistry.

CAS 954239-22-6

6-(trifluoromethyl)-1H-indazole

6-Trifluoromethylindazole

Ref: IN-DA00IJ36

6-(Trifluoromethyl)-1H-indazole

Ref: 54-PC51050

6-(Trifluoromethyl)-1H-indazole

Ref: 10-F220403