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Structure of 154549-38-9
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This boronate moiety features a sterically shielded aryl core, enabling stable coupling in Suzuki-Miyaura reactions under mild conditions. The triisopropyl substituents provide enhanced solubility and resistance to protodeboronation, facilitating efficient cross-coupling with diverse heteroaryl halides.
(2,4,6-Triisopropylphenyl)boronic acid serves as a sterically hindered arylboronic acid that facilitates Suzuki-Miyaura cross-coupling reactions under mild conditions. Its bulky triisopropyl substituents enhance stability and reduce protodeboronation, enabling reliable coupling with diverse electrophiles. The compound exhibits excellent bench stability, ease of handling, and compatibility with sensitive functional groups, making it a practical choice for constructing complex biaryls and heterocyclic scaffolds in medicinal chemistry and materials 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: