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Structure of 916737-77-4
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6-Bromo-3-methoxypyridin-2-amine features a brominated pyridine core with a methoxy group at C3 and an amino substituent at C2, delivering a versatile scaffold for medicinal chemistry. The electron-deficient heterocycle facilitates palladium-catalyzed coupling reactions, while the methoxy moiety enhances solubility and modulates electronic properties. This bench-stable compound serves as a key intermediate in the synthesis of kinase inhibitors and functionalized pharmaceuticals.
6-Bromo-3-methoxypyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromo and amino functionalities. The methoxy group enhances solubility and modulates electronic properties, while the compound exhibits excellent bench stability and compatibility with standard synthetic workflows. Its orthogonally reactive sites facilitate efficient diversification in heterocyclic scaffold development.
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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: