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Structure of 1150114-42-3
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This boronic acid features a pyridine ring functionalized with an isopropoxy group at the 2-position and a boronic acid moiety at the 3-position, enabling efficient Suzuki-Miyaura coupling. The isopropoxy substituent enhances solubility and stability under standard conditions, while the boronic acid group facilitates reliable carbon–carbon bond formation in complex molecule synthesis.
(2-Isopropoxypyridin-3-yl)boronic acid serves as a versatile building block in cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds under standard Suzuki-Miyaura conditions. The isopropoxy group enhances solubility and stability, while the boronic acid functionality offers reliable reactivity with aryl halides and pseudohalides. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for medicinal chemistry campaigns and process-scale synthesis.
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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: