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Structure of 1243174-57-3
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(R)-3-Methyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butan-1-amine hydrochloride features a chiral boronate handle paired with a sterically defined amine side chain. This bench-stable reagent integrates seamlessly into Suzuki-Miyaura coupling workflows, enabling efficient C–C bond formation under mild conditions. The tetramethyl dioxaborolane moiety ensures high functional group tolerance and stability during storage and handling.
(R)-3-Methyl-1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)butan-1-amine hydrochloride serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its chiral tertiary amine functionality enables direct incorporation into bioactive scaffolds, while the tetramethylboronate group offers excellent functional group tolerance and compatibility with standard coupling conditions. The hydrochloride salt enhances solubility and handling, facilitating purification and integration into iterative synthesis 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: