Home Chemistry Organometallic Reagents Organoborons 1-(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Benzyl)Piperazine
Suzuki Coupling: The boron atom in the dioxaborolane can be used for Suzuki coupling reactions with aryl or vinyl halides in the presence of a palladium catalyst to form new carbon-carbon bonds. This reaction is commonly used in organic synthesis to introduce aryl or vinyl groups into molecules.
Amide Formation: The piperazine group can react with acyl chlorides or anhydrides to form amides. This reaction is known as acylation and is often used to modify organic compounds.
Alkylation: The piperazine nitrogen atoms can undergo alkylation reactions with alkyl halides or sulfonates to introduce alkyl groups onto the piperazine ring.
Deboronation: The boron atom in the dioxaborolane can be removed by treatment with acids or other reagents, resulting in the formation of a carbon-carbon bond at the boron-substituted position.
Substitution Reactions: The benzyl group on the piperazine can undergo substitution reactions with various nucleophiles or electrophiles depending on the reaction conditions.
Reductive Amination: The piperazine group can participate in reductive amination reactions, which involve the formation of secondary amines by reacting with carbonyl compounds in the presence of reducing agents.
Hydrolysis: The compound can undergo hydrolysis reactions under acidic or basic conditions, leading to the cleavage of various bonds in the molecule.
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1-(4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazin-1-yl)ethanone
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tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazine-1-carboxylate
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1-Methyl-4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]piperazine
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1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazine dihydrochloride
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1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazine hydrochloride
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