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Structure of 652148-92-0
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2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine features a boronate ester group that enables efficient Suzuki-Miyaura cross-coupling under mild conditions. The electron-deficient pyridine ring enhances reactivity in palladium-catalyzed transformations. This bench-stable reagent integrates seamlessly into complex molecular architectures with high functional group tolerance.
2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile Suzuki-Miyaura coupling partner, enabling efficient C–C bond formation under mild conditions. The boronate group exhibits high stability, excellent functional group tolerance, and compatibility with diverse reaction partners. This reagent facilitates the construction of biaryl architectures in medicinal chemistry and materials science workflows, offering reliable performance and straightforward purification.
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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: