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Structure of 1867923-49-6
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This boronate ester features a cyclopropylvinyl group attached to a tetramethyl-substituted dioxaborolane ring, offering enhanced stability and reactivity in Suzuki-Miyaura coupling. The sterically shielded boron center enables efficient cross-coupling under mild conditions, while the cyclopropylvinyl moiety provides a unique handle for downstream functionalization. Ideal for synthetic applications requiring bench-stable, moisture-tolerant boron reagents.
2-(1-Cyclopropylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its cyclopropylvinyl moiety enables efficient incorporation into conjugated systems and heterocyclic scaffolds, with the tetramethyl-substituted dioxaborolane core offering enhanced stability and compatibility with diverse functional groups. The compound facilitates mild reaction conditions and straightforward purification, making it ideal for iterative synthesis in medicinal chemistry and materials development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: