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Structure of 313545-20-9
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3-Chloro-2-methylphenylboronic acid features a boronic acid group appended to a chlorinated, methyl-substituted phenyl ring. This configuration enhances stability and reactivity in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under standard conditions. The ortho-chloro substituent facilitates further functionalization, while the methyl group provides steric and electronic modulation.
3-Chloro-2-methylphenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its stability, ease of handling, and compatibility with diverse functional groups make it well-suited for the synthesis of biaryl scaffolds in pharmaceutical and agrochemical research.
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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: