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Structure of 942438-89-3
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3-Chloro-2-methoxypyridine-5-boronic acid features a pyridine scaffold bearing a boronic acid group at the 5-position and complementary substituents at the 3-chloro and 2-methoxy sites. This configuration enables direct incorporation into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering functionalized heterocycles with high chemoselectivity. The methoxy group enhances solubility in polar solvents, while the chloropyridine moiety provides a handle for further derivatization. This compound serves as a key intermediate in the synthesis of bioactive molecules and advanced materials.
3-Chloro-2-methoxypyridine-5-boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The boronic acid functionality offers excellent bench stability and compatibility with diverse reaction conditions, while the chloro and methoxy groups provide orthogonal reactivity for sequential functionalization. This compound facilitates rapid access to complex pyridine-based scaffolds relevant to medicinal chemistry and materials science.
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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: