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Structure of 14559-88-7
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This boronate moiety features a terminal alkenyl group enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. The (2-methylprop-1-en-1-yl)boronic acid delivers high functional group tolerance and stability under standard bench conditions, streamlining the synthesis of conjugated olefinic architectures in complex molecular frameworks.
(2-Methylprop-1-en-1-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its terminal alkene functionality offers high chemoselectivity and compatibility with diverse functional groups, facilitating the synthesis of conjugated systems and complex molecular architectures. The boronic acid moiety ensures excellent bench stability and ease of purification, making it ideal for iterative synthetic strategies 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: