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Structure of 851756-57-5
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This boronic acid features a methoxy-substituted aryl ring flanked by two chlorine atoms at the 2 and 6 positions, delivering enhanced stability and predictable reactivity in Suzuki-Miyaura coupling. The electron-withdrawing chlorines modulate nucleophilicity while the methoxy group improves solubility and facilitates downstream functionalization.
(2,6-dichloro-3-methoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its stability under ambient conditions and tolerance to various functional groups facilitate straightforward purification and integration into complex molecular architectures. The dichloro substitution pattern enhances electrophilic reactivity in downstream transformations, while the methoxy group provides directional control in regioselective coupling processes.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: