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Structure of 2411223-34-0
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tert-Butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-azaspiro[3.4]oct-6-ene-2-carboxylate delivers a sterically protected boronate handle integrated into a rigid spirocyclic scaffold. This bench-stable reagent enables efficient Suzuki-Miyaura coupling under mild conditions, facilitating rapid access to complex nitrogen-containing architectures in medicinal chemistry and materials synthesis.
tert-Butyl 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-azaspiro[3.4]oct-6-ene-2-carboxylate serves as a versatile boron-containing building block for Suzuki-Miyaura coupling reactions. The spirocyclic scaffold provides structural rigidity and stereochemical control, while the tert-butyl ester offers stability and straightforward deprotection. Its compatibility with diverse reaction conditions enables efficient construction of complex heterocyclic architectures and functionalized scaffolds in medicinal chemistry and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: