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Structure of 779331-47-4
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This boronic acid features a benzyloxy-substituted fluorophenyl scaffold, enabling efficient cross-coupling reactions under standard conditions. The electron-deficient aryl group enhances reactivity in Suzuki-Miyaura processes, while the bench-stable boronate moiety simplifies handling and storage.
(2-(Benzyloxy)-5-fluorophenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The boronic acid functionality exhibits excellent bench stability and tolerates a range of functional groups, facilitating the synthesis of substituted biaryls and complex heterocyclic scaffolds. Its benzyloxy and fluorine substituents provide orthogonal reactivity handles and enhanced metabolic stability, making it particularly valuable in medicinal chemistry and API intermediate development.
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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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: