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Structure of 1008415-02-8
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(3-Chloro-4-cyanophenyl)boronic acid features a boronic acid handle appended to a chlorinated and cyano-substituted aromatic ring, enabling efficient Suzuki-Miyaura coupling under standard conditions. The electron-withdrawing cyano group enhances reactivity while the chlorine substituent offers orthogonal functionalization potential. This compound delivers high stability and predictable transformation in synthetic workflows.
(3-Chloro-4-cyanophenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The ortho-chloro and cyano groups provide orthogonal reactivity for downstream functionalization, while the boronic acid moiety offers excellent bench stability and ease of purification. Widely used in pharmaceutical and agrochemical synthesis, it functions reliably in the construction of substituted biaryl and heteroaryl 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: