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Structure of 1443380-14-0
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This boronate moiety enables direct coupling in Suzuki-Miyaura reactions, offering enhanced reactivity and stability under standard conditions. The fluorinated pyridine scaffold provides favorable electronic tuning, while the methoxy group improves solubility and reduces aggregation during synthesis.
(6-Fluoro-2-methoxypyridin-3-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. The fluorine and methoxy groups provide orthogonal reactivity and enhanced stability, while the boronic acid functionality facilitates reliable coupling under mild conditions. Its bench-stable nature and compatibility with diverse functional groups make it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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: