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Structure of 913835-32-2
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5-Borono-2-chlorobenzoic acid features a boronate group positioned ortho to a chlorinated benzene ring, enabling selective coupling in Suzuki-Miyaura reactions. The carboxylic acid functionality provides solubility and handles well under standard conditions. This compound integrates readily into bioactive scaffolds requiring halogenated aryl boronates.
5-Borono-2-chlorobenzoic acid serves as a versatile building block in transition-metal-catalyzed coupling reactions, particularly Suzuki-Miyaura cross-couplings. The boronic acid group enables efficient C–C bond formation under mild conditions, while the ortho-chloro and carboxylic acid functionalities provide orthogonal reactivity for further derivatization. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthesis of complex heterocycles and pharmaceutical scaffolds.
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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: