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Structure of 936249-33-1
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This boronate moiety integrates a chloro and cyano group at ortho positions, enabling selective cross-coupling under standard conditions. The electron-deficient aryl system enhances reactivity in Suzuki-Miyaura transformations while maintaining bench-stable handling.
(2-Chloro-5-cyanophenyl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. The pendant chloro and cyano groups provide orthogonal reactivity for downstream functionalization, while the boronic acid moiety offers excellent bench stability and ease of purification. Its compatibility with diverse reaction partners makes it a reliable scaffold for constructing complex aryl architectures in medicinal chemistry and materials science 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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: