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Structure of 693774-10-6
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This pyridine boronate features a sterically hindered 2,6-dimethyl substitution pattern that enhances stability and minimizes undesired side reactions. The tetramethylborolane moiety enables efficient coupling under mild conditions, making it ideal for Suzuki-Miyaura cross-coupling applications in complex molecule synthesis.
2,6-Dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-methyl groups enhance regioselectivity and electronic modulation in heterocyclic coupling, while the sterically protected boronate moiety ensures excellent shelf stability and compatibility with diverse functional groups. Ideal for constructing complex pyridine-based scaffolds in medicinal chemistry and materials science applications.
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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: