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Structure of 1313617-76-3
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This boronic acid features a methoxy-substituted aromatic ring paired with a methyl group at the ortho position, enhancing electronic and steric control. The pendant boronate moiety enables efficient Suzuki-Miyaura coupling under standard conditions, delivering high yields in cross-coupling reactions. Designed for stability and ease of handling, it integrates seamlessly into complex molecule synthesis workflows.
(3-Methoxy-2-methylphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. Its ortho-substituted arylboronic acid structure provides enhanced stability and predictable reactivity, facilitating the construction of complex biaryl architectures. The methoxy and methyl groups offer complementary electronic and steric modulation, supporting functional group tolerance and ease of purification—key advantages for medicinal chemistry and process-scale synthesis.
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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: