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Structure of 1072945-98-2
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized pyridine derivatives with high efficiency. The para-chloro and methoxy substituents provide orthogonal reactivity and enhanced solubility, enabling streamlined synthesis of complex heterocyclic scaffolds.
(2-Chloro-5-methoxypyridin-4-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The chloropyridine moiety offers orthogonal reactivity for downstream functionalization, while the boronic acid group provides excellent bench stability and compatibility with diverse reaction conditions. Its methoxy substituent enhances solubility and modulates electronic properties, making it well-suited for medicinal chemistry applications and scale-up processes.
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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-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: