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Structure of 182344-13-4
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This boronic acid features a chlorinated hydroxyphenyl scaffold enabling direct functionalization in cross-coupling reactions. The ortho-hydroxyl group enhances solubility and facilitates chelation, while the chlorine substituent provides a handle for further derivatization. Bench-stable under standard conditions, it integrates efficiently into complex molecule synthesis workflows.
(3-Chloro-4-hydroxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds with high functional group tolerance. The ortho-chloro and phenolic hydroxyl groups provide strategic handles for further derivatization, while the boronic acid moiety offers excellent bench stability and ease of purification. This compound functions reliably in both solution-phase and solid-phase synthesis workflows.
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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: