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Structure of 77476-95-0
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5-Bromo-N-isopropylpyrimidin-2-amine features a bromine atom at the 5-position and a sterically hindered isopropyl group attached to the pyrimidine nitrogen, delivering enhanced stability and tunable reactivity. This scaffold integrates readily into pharmaceutical intermediates and functional materials, offering robust performance under standard bench conditions.
5-Bromo-N-isopropylpyrimidin-2-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to construct functionalized pyrimidine scaffolds. The bromine atom facilitates efficient Suzuki, Stille, or Negishi couplings, while the N-isopropyl group enhances solubility and modulates electronic properties. Bench-stable and readily purified by column chromatography, it functions reliably in multi-step syntheses of kinase inhibitors and other bioactive heterocycles.
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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-H319
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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: