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Structure of 179898-50-1
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This boronic acid features a chlorinated, methoxy-substituted phenyl core that enhances electronic tuning and stability. The boronate moiety integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, delivering high yields with minimal protodeboronation. Its bench-stable nature simplifies handling in synthetic workflows.
(3-Chloro-2-methoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The chloro and methoxy groups provide orthogonal reactivity and enhanced solubility, while the boronic acid moiety offers excellent bench stability and compatibility with diverse functional groups. Its predictable performance facilitates rapid access to substituted biaryl scaffolds relevant to pharmaceutical and agrochemical synthesis.
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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: