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Structure of 1060815-72-6
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2-Bromo-5-chloropyridin-4-amine features a pyridine core functionalized with bromo and chloro substituents at the 2- and 5-positions, respectively, and a primary amine group at the 4-position. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct coupling reactions under palladium catalysis. The molecule exhibits good stability under standard handling conditions and integrates readily into complex scaffolds for drug discovery programs.
2-Bromo-5-chloropyridin-4-amine serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its dual halogen substituents enable selective cross-coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig couplings, facilitating the construction of complex biaryl and amine-containing scaffolds. The pyridinamine functionality provides a handle for further derivatization, while the compound exhibits sufficient bench stability for routine handling and purification.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P301+P310-P330-P405-P501
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Lot numbers can be found on the outside label of a product: