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Structure of 4151-80-8
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Reactant involved in synthesis of:Organic field-effect transistors based on organic semiconductors containing diazaborolesCycloparaphenylenes via Suzuki coupling1,3,2-Diazaboroine derivatives for organic thin-film transistor applicationsBack-to-back coupled 2,6-bis(triazol-1-yl)pyridine moleculesRectangular host via electrochemical reactions with methylaquacobaloxime and diamineArylboronates from reactions with catechol, dihydroxynaphthalene and diaminobenzenedithiol for use as organic field-effect transistors and light emitting diodes
[1,1'-Biphenyl]-4,4'-diyldiboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl and polyaryl scaffolds. Its dual boronic acid functionality offers enhanced reactivity and orthogonality in sequential coupling processes, while maintaining excellent bench stability and ease of purification—key attributes for scalable synthesis and medicinal chemistry 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: