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Structure of 1571135-77-7
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This boronate moiety features a difluoromethylpyridine scaffold, delivering enhanced stability and compatibility in cross-coupling reactions. The electron-deficient pyridine ring enables efficient palladium-catalyzed transformations, while the bench-stable boronic acid functionality simplifies handling and integration into complex molecular architectures.
(2-(Difluoromethyl)pyridin-4-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. The difluoromethyl group imparts enhanced metabolic stability and modulates electronic properties, while the pyridine moiety provides a handle for further functionalization. Bench-stable and compatible with a broad range of reaction conditions, it facilitates the synthesis of complex heterocyclic scaffolds relevant to medicinal chemistry and agrochemical development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: