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Structure of 1106676-82-7
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This boronate reagent features a strategically positioned bromine and two fluorine substituents that enhance its stability and modulate electronic properties. The para-fluorinated aryl group enables efficient cross-coupling under standard conditions, while the ortho-bromo functionality facilitates downstream functionalization. Designed for precision in complex synthesis, this bench-stable reagent integrates seamlessly into iterative coupling sequences.
(4-Bromo-2,5-difluorophenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation with aryl and vinyl halides. Its stability under ambient conditions, compatibility with diverse functional groups, and predictable reactivity make it ideal for constructing complex molecular architectures in medicinal chemistry and materials science.
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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: