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Structure of 870822-86-9
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(6-Chloronaphthalen-2-yl)boronic acid features a chlorinated naphthalene scaffold bearing a boronic acid group at the 6-position, enabling efficient Suzuki-Miyaura cross-coupling reactions. This bench-stable reagent integrates readily into complex molecular architectures, offering predictable regioselectivity and compatibility with diverse reaction conditions.
(6-Chloronaphthalen-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation with aryl and heteroaryl halides. The chloro substituent provides orthogonal reactivity for downstream functionalization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction conditions. Its utility in constructing biaryl scaffolds makes it a reliable reagent for pharmaceutical and materials chemistry applications.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: