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Structure of 913835-71-9
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This boronic acid features a chloro-substituted aromatic ring paired with a hydroxyl group and a boronate moiety, enabling efficient Suzuki-Miyaura coupling under standard conditions. The ortho-chlorine facilitates directed functionalization, while the hydroxyl group enhances solubility and stability in aqueous-organic mixtures.
(2-Chloro-5-hydroxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The ortho-chloro and phenolic hydroxyl groups provide orthogonal reactivity for downstream functionalization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction setups. Its utility is well-documented in the synthesis of substituted aryl 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: