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Structure of 1029439-83-5
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2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol features a boronate ester group flanked by two fluorine atoms at the 2 and 6 positions, enhancing stability and reactivity in Suzuki-Miyaura coupling. This bench-stable arylboron reagent integrates readily into complex molecular architectures, enabling efficient C–C bond formation under mild conditions.
2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The difluorophenyl moiety enhances metabolic stability and modulates electronic properties, while the pinacol boronate group ensures excellent bench stability, ease of handling, and compatibility with a broad range of coupling partners. Its ortho-fluorine substituents enable selective functionalization in complex molecule synthesis, making it a valuable scaffold for pharmaceutical and agrochemical discovery.
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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: