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Structure of 1377152-43-6
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2-(2-Fluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a bench-stable boronate reagent featuring a fluorinated styrenyl moiety. This electrophilic handle enables efficient Suzuki-Miyaura coupling under mild conditions, offering enhanced compatibility with sensitive functional groups. The tetramethyl-substituted dioxaborolane ring ensures high stability and low hydrolytic reactivity, facilitating reliable handling in aqueous or protic solvents.
2-(2-Fluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for palladium-catalyzed cross-coupling reactions. It enables efficient construction of ortho-fluorinated styrenyl motifs in complex molecules, offering excellent functional group tolerance and compatibility with standard Suzuki-Miyaura coupling conditions. Its tetramethyl-substituted dioxaborolane core ensures high stability and ease of purification, making it ideal for iterative synthesis 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: