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Structure of 870521-30-5
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This boronate moiety integrates a pyridine scaffold with an isopropoxy substituent, enhancing solubility and stability in polar solvents. The para-positioned boronic acid enables efficient Suzuki-Miyaura coupling under mild conditions, while the electron-deficient pyridine ring facilitates directed functionalization. Ideal for constructing bioactive heterocycles and advanced intermediates in medicinal chemistry workflows.
(6-Isopropoxypyridin-3-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. The isopropoxy group enhances solubility and stability compared to simpler alkoxy analogs, while the boronic acid functionality facilitates reliable coupling under standard Suzuki-Miyaura conditions. Its ortho-directed electronic profile supports predictable regioselectivity in complex molecule assembly.
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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: