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Structure of 2377607-88-8
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This boronate moiety features a chlorinated thiazole ring, enhancing electronic modulation and stability. It integrates efficiently into Suzuki-Miyaura coupling reactions under standard conditions, delivering robust yields with minimal protodeboronation. The electron-deficient heterocycle enables selective functionalization in complex synthesis workflows.
(2-Chlorothiazol-5-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient access to functionalized thiazole scaffolds. Its boronic acid group facilitates Suzuki-Miyaura coupling under mild conditions, while the 2-chloro substituent offers orthogonal reactivity for further derivatization. The compound exhibits good bench stability and is compatible with diverse functional groups, making it well-suited for medicinal chemistry and process development workflows.
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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: