Home Chemistry Organometallic Reagents Organoborons 2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridine
Suzuki-Miyaura Coupling: This compound can undergo Suzuki-Miyaura coupling reactions with aryl halides or pseudohalides in the presence of a palladium catalyst. This reaction is commonly used to form carbon-carbon bonds.
Boronic Acid Derivatives: The boron atom in the molecule can be converted into various boronic acid derivatives, such as boronic esters or boronic acids. These derivatives can participate in further reactions, such as cross-coupling reactions or transition metal-catalyzed reactions.
Oxidation: The boron atom in the compound can be oxidized to form a boronic acid or boronate ester, depending on the reaction conditions. This oxidation can be achieved using reagents like hydrogen peroxide or alkaline hydrogen peroxide.
Hydroboration: The compound can undergo hydroboration reactions, where boron adds to an alkene or alkyne in the presence of a boron source and a reducing agent. This can lead to the formation of boron-containing organic compounds.
Boronate Complex Formation: This compound can form boronate complexes with Lewis bases, such as diols or amines. These complexes can serve as intermediates in various reactions.
Cross-Coupling Reactions: The boron atom in the compound can participate in cross-coupling reactions with various electrophiles, including halides and triflates, in the presence of appropriate catalysts.
Functional Group Transformations: The pyridine ring in the molecule can undergo various functional group transformations, including substitution reactions or oxidation reactions.
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2-Bromo-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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2-Methoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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6-Cyanopyridine-2-boronic Acid Pinacol Ester
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2-Fluoro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)pyridine
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