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Structure of 612833-37-1
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This boronic acid features a cyano group at the 5-position and a methoxy substituent at the 2-position, delivering enhanced stability and solubility in polar solvents. The electron-withdrawing cyano moiety modulates reactivity, enabling efficient Suzuki-Miyaura coupling under mild conditions. Designed for streamlined synthesis of functionalized biaryls and heterocycles in medicinal chemistry and materials science.
(5-Cyano-2-methoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl scaffolds with enhanced solubility and stability. The cyano and methoxy groups provide orthogonal functional handles for downstream derivatization, while the boronic acid moiety exhibits excellent bench stability and compatibility with diverse reaction conditions. Its predictable reactivity and ease of purification make it a reliable choice 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: