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Structure of 882678-96-8
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2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline features a boronate ester group enabling efficient Suzuki-Miyaura coupling under mild conditions. The electron-rich aniline moiety enhances reactivity, while the tetramethyl-substituted dioxaborolane imparts excellent stability and moisture tolerance. This bench-stable building block streamlines access to functionalized biaryls in medicinal chemistry and materials synthesis.
2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline serves as a versatile boron-containing building block in palladium-catalyzed cross-coupling reactions. Its stable boronate ester group enables efficient Suzuki-Miyaura coupling with aryl and heteroaryl halides, facilitating the construction of biaryl and extended conjugated systems. The molecule exhibits excellent bench stability, minimal protodeboronation, and compatibility with diverse functional groups, making it ideal for iterative synthesis workflows in medicinal chemistry and materials science.
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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: