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Structure of 957061-05-1
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3-Borono-5-chlorobenzoic acid features a boronate group flanked by a chloro substituent and carboxylic acid functionality, enabling selective coupling in Suzuki-Miyaura reactions. This electron-deficient arylboronic acid delivers high reactivity under mild conditions, offering precise control in C–C bond formation. The combination of steric and electronic tuning enhances stability and functional group compatibility.
3-Borono-5-chlorobenzoic acid serves as a versatile building block in transition-metal-catalyzed coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its boronic acid functionality facilitates Suzuki-Miyaura couplings under mild conditions, while the ortho-chloro and carboxylic acid groups provide orthogonal handles for further functionalization. The compound exhibits good bench stability and is compatible with diverse reaction conditions, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07,GHS08
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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-H312-H315-H319-H332-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: