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Structure of 475275-69-5
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5-Chloro-2-methoxypyridin-4-yl-4-boronic acid features a pyridine core functionalized with chlorine, methoxy, and boronic acid groups, enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. The electron-deficient arylboronate facilitates efficient C–C bond formation under mild conditions. This bench-stable reagent delivers high chemoselectivity in complex molecule synthesis.
5-Chloro-2-methoxypyridin-4-yl-4-boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation with aryl and heteroaryl halides. The pyridine core provides orthogonal reactivity, while the methoxy group enhances solubility and modulates electronic properties. Bench-stable and readily purified by recrystallization, it facilitates scalable synthesis of functionalized pyridine scaffolds relevant to medicinal chemistry and agrochemical development.
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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: