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Structure of 1214264-88-6
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This boronate-functionalized naphthodiazaborinine integrates a stable tetramethylborolane moiety, enabling efficient Suzuki-Miyaura cross-coupling under mild conditions. The fused heterocyclic scaffold enhances electronic stability and facilitates selective functionalization in complex molecular architectures.
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. Its stable dioxaborolane moiety enables efficient C–C bond formation under mild conditions, while the fused diazaborinine scaffold provides enhanced thermal stability and compatibility with diverse functional groups. This reagent facilitates the construction of complex polycyclic architectures commonly found in pharmaceutical and materials chemistry applications.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: