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Structure of 697739-24-5
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2-Chloro-6-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine features a boronate ester group enabling efficient Suzuki-Miyaura coupling under mild conditions. The electron-deficient pyridine core enhances reactivity, while the methoxy substituent improves solubility and stability. This bench-stable reagent streamlines access to functionalized heterocycles in medicinal chemistry and materials synthesis.
2-Chloro-6-methoxy-4-(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 ester group exhibits excellent stability and functional group tolerance, while the chloropyridine moiety facilitates selective cross-coupling with aryl, heteroaryl, and vinyl partners. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical building block for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science.
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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: