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Structure of 845457-55-8
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions, delivering functionalized biaryls with high efficiency. The 3-methyl substituent enhances stability and solubility in common organic solvents, enabling straightforward handling under standard conditions.
(3-Methylbenzofuran-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl architectures. Its bench-stable nature and tolerance to diverse functional groups facilitate reliable synthesis of complex heterocyclic scaffolds. The boronic acid moiety reacts predictably with aryl halides under palladium catalysis, offering high yields and broad scope 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: