The chemical substance known as 4-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]methyl}pyridine, with the CAS number 864754-20-1, is characterized by its complex molecular structure, which includes a pyridine ring and a pyrazole moiety linked through a methylene bridge. The presence of the boron-containing dioxaborolane group contributes to its potential applications in organic synthesis and medicinal chemistry, particularly in the development of boron-based compounds for drug discovery. This compound is likely to exhibit unique reactivity due to the boron atom, which can participate in various chemical transformations, including cross-coupling reactions. Additionally, the presence of multiple functional groups suggests that it may have specific interactions with biological targets, making it of interest in pharmacological studies. Its solubility, stability, and reactivity will depend on the solvent and conditions used, which are critical for its application in research and industry. Overall, this compound represents a versatile building block in the field of organic chemistry.

4-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]methyl}pyridine

864754-20-1: The chemical substance known as 4-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]methyl}pyridine, with the CAS number 864754-20-1, is characterized by its complex molecular structure, which includes a pyridine ring and a pyrazole moiety linked through a methylene bridge. The presence of the boron-containing dioxaborolane group contributes to its potential applications in organic synthesis and medicinal chemistry, particularly in the development of boron-based compounds for drug discovery. This compound is likely to exhibit unique reactivity due to the boron atom, which can participate in various chemical transformations, including cross-coupling reactions. Additionally, the presence of multiple functional groups suggests that it may have specific interactions with biological targets, making it of interest in pharmacological studies. Its solubility, stability, and reactivity will depend on the solvent and conditions used, which are critical for its application in research and industry. Overall, this compound represents a versatile building block in the field of organic chemistry.

CAS 864754-20-1

4-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]methyl}pyridine

4-((4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine

Ref: IN-DA003JXF

1-(4-Pyridinomethyl)pyrazole-4-boronic acid, pinacol ester

Ref: 54-OR361573

1-(Pyridin-4-ylmethyl)-1H-pyrazole-4-boronic acid pinacol ester

Ref: 10-F047716