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Structure of 1083168-95-9
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This boronate ester features a 5-fluoro-2-methoxy-3-pyridyl scaffold, enabling efficient cross-coupling under standard conditions. The tetramethyl-substituted dioxaborolane group enhances stability and reactivity, facilitating direct incorporation into complex molecular architectures via palladium-catalyzed transformations.
5-Fluoro-2-methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyridine core enables transition-metal-catalyzed C–C bond formation, while the 5-fluoro and 2-methoxy substituents provide orthogonal reactivity and electronic tuning. The pinacol boronate group offers excellent bench stability, ease of purification, and compatibility with a broad range of coupling partners, facilitating efficient synthesis of substituted heterocycles and complex pharmaceutical scaffolds.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: