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Structure of 148214-56-6
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5-Bromo-2-methoxypyrimidin-4-amine integrates a bromine atom at the 5-position and a methoxy group at the 2-position, delivering a versatile scaffold for nucleophilic substitution and cross-coupling reactions. The electron-deficient pyrimidine core pairs with the amine functionality to enable efficient derivatization in medicinal chemistry and agrochemical synthesis.
5-Bromo-2-methoxypyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromine and amine groups offer orthogonal reactivity for sequential derivatization, while the methoxy substituent enhances solubility and modulates electronic properties. Bench-stable and readily purified by flash chromatography, it facilitates the construction of pyrimidine-based scaffolds prevalent in kinase inhibitors and antiviral agents.
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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: