1H-Pyrrolo[2,3-b]pyridine, 2-methyl-1-(phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a complex organic compound characterized by its unique bicyclic structure, which combines a pyrrole and pyridine moiety. This compound features a sulfonyl group, which enhances its reactivity and solubility in various solvents, making it useful in synthetic organic chemistry. The presence of the dioxaborolane group suggests potential applications in boron chemistry, particularly in cross-coupling reactions and as a reagent in organic synthesis. The tetramethyl substitution on the dioxaborolane ring contributes to steric hindrance, which can influence the compound's reactivity and selectivity in chemical reactions. Additionally, the compound's molecular structure may exhibit interesting electronic properties due to the conjugation between the aromatic systems and the heteroatoms. Overall, this compound is of interest in medicinal chemistry and materials science, where its unique structural features can be exploited for the development of new pharmaceuticals or functional materials.

1H-PYRROLO[2,3-B]PYRIDINE, 2-METHYL-1-(PHENYLSULFONYL)-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-

1014613-31-0: 1H-Pyrrolo[2,3-b]pyridine, 2-methyl-1-(phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is a complex organic compound characterized by its unique bicyclic structure, which combines a pyrrole and pyridine moiety. This compound features a sulfonyl group, which enhances its reactivity and solubility in various solvents, making it useful in synthetic organic chemistry. The presence of the dioxaborolane group suggests potential applications in boron chemistry, particularly in cross-coupling reactions and as a reagent in organic synthesis. The tetramethyl substitution on the dioxaborolane ring contributes to steric hindrance, which can influence the compound's reactivity and selectivity in chemical reactions. Additionally, the compound's molecular structure may exhibit interesting electronic properties due to the conjugation between the aromatic systems and the heteroatoms. Overall, this compound is of interest in medicinal chemistry and materials science, where its unique structural features can be exploited for the development of new pharmaceuticals or functional materials.

CAS 1014613-31-0

1H-PYRROLO[2,3-B]PYRIDINE, 2-METHYL-1-(PHENYLSULFONYL)-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-

1H-Pyrrolo[2,3-b]pyridine, 2-methyl-1-(phenylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

Ref: IN-DA0004IO