(5-Iodopyrrolo[2,3-b]pyridin-1-yl)-triisopropyl-silane is a chemical compound characterized by its unique structure, which includes a pyrrolo[2,3-b]pyridine core substituted with an iodine atom at the 5-position and a triisopropylsilyl group. This compound is notable for its potential applications in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the iodine atom can enhance reactivity, making it useful in various coupling reactions, while the triisopropylsilyl group serves as a protective or stabilizing moiety, facilitating further functionalization. The compound is likely to exhibit properties typical of organosilicon compounds, such as hydrophobicity and thermal stability. Additionally, its molecular structure suggests potential interactions with biological targets, which may be explored in drug discovery contexts. As with many organoiodine compounds, it may also exhibit interesting electronic properties due to the halogen substitution. Safety and handling precautions should be observed, as with all chemical substances, particularly those containing halogens and organosilicon functionalities.

(5-iodopyrrolo[2,3-b]pyridin-1-yl)-triisopropyl-silane

913983-21-8: (5-Iodopyrrolo[2,3-b]pyridin-1-yl)-triisopropyl-silane is a chemical compound characterized by its unique structure, which includes a pyrrolo[2,3-b]pyridine core substituted with an iodine atom at the 5-position and a triisopropylsilyl group. This compound is notable for its potential applications in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. The presence of the iodine atom can enhance reactivity, making it useful in various coupling reactions, while the triisopropylsilyl group serves as a protective or stabilizing moiety, facilitating further functionalization. The compound is likely to exhibit properties typical of organosilicon compounds, such as hydrophobicity and thermal stability. Additionally, its molecular structure suggests potential interactions with biological targets, which may be explored in drug discovery contexts. As with many organoiodine compounds, it may also exhibit interesting electronic properties due to the halogen substitution. Safety and handling precautions should be observed, as with all chemical substances, particularly those containing halogens and organosilicon functionalities.

CAS 913983-21-8

(5-iodopyrrolo[2,3-b]pyridin-1-yl)-triisopropyl-silane