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Structure of 1238196-66-1
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This boronate moiety features a para-chlorinated hydroxyphenyl scaffold, enabling efficient coupling in Suzuki-Miyaura reactions. The electron-deficient aryl ring enhances reactivity, while the bench-stable boronic acid functionality simplifies handling and integration into complex synthetic sequences.
(4-Chloro-2-hydroxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The boronic acid functionality exhibits good bench stability and compatibility with diverse functional groups, facilitating the construction of substituted biaryls and heterocyclic scaffolds relevant to medicinal chemistry and materials science.
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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: