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Structure of 560132-24-3
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This boronate moiety features a sterically hindered tert-butyl group that enhances stability and solubility in organic media. It integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, enabling efficient C–C bond formation with aryl halides. The para-substituted phenyl ring provides electronic tuning for controlled reactivity.
(3-(tert-Butyl)phenyl)boronic acid serves as a robust building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds under mild conditions. Its tert-butyl substituent enhances steric stability and improves bench storage longevity. The boronic acid functionality exhibits high functional group tolerance and facilitates straightforward purification via crystallization or flash chromatography, making it well-suited for iterative synthesis in medicinal chemistry and process development 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: