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Structure of 1251537-39-9
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This boronate ester features a tert-butoxycarbonyl-protected piperidinyl scaffold, enabling stable incorporation into complex molecular architectures. The pendant boronic acid group facilitates efficient Suzuki-Miyaura cross-coupling reactions under mild conditions. Designed for synthetic versatility in medicinal chemistry and process development workflows, this reagent combines robustness with high functional group tolerance.
(1-(Tert-butoxycarbonyl)piperidin-4-yl)boronic acid serves as a stable, bench-accessible building block for the synthesis of piperidine-containing scaffolds. It facilitates Suzuki-Miyaura cross-coupling reactions with broad functional group tolerance, enabling efficient construction of complex heterocycles and biologically relevant frameworks. The tert-butyl carbamate protecting group ensures compatibility with standard reaction conditions and simplifies purification.
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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 : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: