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Structure of 161344-84-9
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(4S,5S)-2-butyl-N⁴,N⁴,N⁵,N⁵-tetramethyl-1,3,2-dioxaborolane-4,5-dicarboxamide serves as a stable, bench-ready boronate building block for Suzuki-Miyaura coupling reactions. Its stereodefined dioxaborolane core enables predictable regioselective cross-coupling with aryl and vinyl halides, while the N⁴,N⁴,N⁵,N⁵-tetramethyl substitution enhances hydrolytic stability and facilitates purification. The butyl substituent provides enhanced solubility in organic media, making it well-suited for iterative synthesis of complex heterocyclic scaffolds and API intermediates.
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Lot numbers can be found on the outside label of a product: