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Structure of 73852-17-2
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2,6-Dichlorophenylboronic acid features a boronate moiety flanked by two chlorine atoms at the 2 and 6 positions of the phenyl ring, delivering enhanced stability and controlled reactivity. This electron-deficient arylboronic acid integrates efficiently into Suzuki-Miyaura coupling reactions, enabling reliable carbon-carbon bond formation under mild conditions. Its bench-stable nature simplifies handling and storage in synthetic workflows.
2,6-Dichlorophenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-dichloro substitution enhances stability and modulates reactivity, while the boronic acid group offers excellent functional group tolerance and ease of purification. This reagent is well-suited for constructing biaryl scaffolds in medicinal chemistry and materials science applications.
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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: