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Structure of 919347-67-4
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This boronate moiety integrates a tert-butoxycarbonyl-protected piperazine ring at the 6-position of a pyridine scaffold, enabling facile downstream functionalization. The electron-deficient pyridine core enhances reactivity in Suzuki-Miyaura couplings, while the bench-stable boronic acid group tolerates standard handling conditions and moisture exposure.
(6-(4-(tert-Butoxycarbonyl)piperazin-1-yl)pyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The protected piperazine moiety offers enhanced stability and orthogonal deprotection compatibility, while the boronic acid functionality facilitates reliable coupling with aryl halides and triflates. Its bench-stable solid form simplifies handling and purification, making it well-suited for iterative synthesis of complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P233-P260-P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: