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Structure of 458532-84-8
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2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine features a boronate ester group that enables efficient Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances stability and reactivity under standard conditions. This pyridine derivative serves as a key building block for functionalized heterocycles in medicinal chemistry and materials science applications.
2-Chloro-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 group exhibits excellent stability, tolerates diverse functional groups, and facilitates rapid purification. Its pyridine scaffold provides a valuable building block for constructing bioactive heterocycles, pharmaceutical intermediates, and conjugated materials in medicinal chemistry and materials science workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H320
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Precautionary Statements : P264-P270-P301+P310-P305+P351+P338-P330-P337+P313-P405-P501
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Lot numbers can be found on the outside label of a product: