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Structure of 936618-92-7
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This boronate ester features a 3-fluorophenyl moiety integrated via a stable dioxaborolane ring, enabling efficient Suzuki-Miyaura coupling under standard conditions. The tetramethyl substitution enhances stability and solubility in organic solvents, while the fluorine atom imparts electronic modulation for selective cross-coupling reactions.
2-(3-Fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its fluorinated aryl group enables selective functionalization in medicinal chemistry workflows, while the tetramethyl-substituted dioxaborolane core ensures high chemical stability and excellent functional group tolerance. The compound facilitates efficient C–C bond formation under mild conditions, making it ideal for constructing complex biaryl architectures in API development and synthetic route optimization.
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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: