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Structure of 1310384-35-0
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This boronate ester features a 3-fluoro-2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine scaffold, combining electron-deficient pyridine reactivity with a stable, moisture-tolerant boronate handle. The para-substituted dioxaborolane integrates readily into Suzuki-Miyaura cross-coupling reactions under mild conditions, enabling efficient C–C bond formation in complex molecular architectures.
3-Fluoro-2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile Suzuki-Miyaura coupling partner, enabling efficient C–C bond formation under mild conditions. The boronate ester group exhibits excellent stability and compatibility with diverse functional groups, while the fluorine and methoxy substituents provide orthogonal reactivity for downstream modifications. Its bench-stable nature and predictable coupling efficiency make it ideal for constructing complex heterocyclic architectures 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: