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Structure of 893440-50-1
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3-Amino-2-methoxy-5-(4,4,5,5-tetramethyl[1,3,2-dioxaborolan-2-yl)pyridine features a boronate ester handle paired with an electron-rich pyridine core, enabling efficient Suzuki-Miyaura coupling under mild conditions. The methoxy and amino substituents enhance solubility and reactivity, while the tetramethyl dioxaborolane moiety ensures stability during storage and handling. This compound integrates seamlessly into complex molecular architectures requiring precise C–C bond formation.
3-Amino-2-methoxy-5-(4,4,5,5-tetramethyl[1,3,2-dioxaborolan-2-yl)pyridine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pinacol boronate group enables stable, air-tolerant handling and facilitates efficient coupling with aryl halides and triflates under mild conditions. The amino and methoxy substituents provide orthogonal reactivity and tune electronic properties, making this compound well-suited for the synthesis of functionalized heterocyclic scaffolds in medicinal chemistry and materials science applications.
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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: