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Structure of 2305022-53-9
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions, delivering functionalized naphthalene derivatives with high efficiency. The chlorine substituent enhances reactivity and enables sequential transformations, while the bench-stable nature simplifies handling in synthetic workflows.
(8-Chloronaphthalen-1-yl)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 boronic acid functionality exhibits good bench stability and compatibility with diverse functional groups, facilitating the synthesis of complex biaryl systems relevant to pharmaceutical and materials chemistry. The chlorine substituent provides orthogonal reactivity for further functionalization.
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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: