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Structure of 36314-97-3
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4-Chloro-6-phenylpyrimidin-2-amine features a pyrimidine core functionalized with a chloro group at C4 and a phenyl ring at C6, enabling integration into kinase inhibitor scaffolds. The amine at C2 facilitates coupling reactions, while the electron-withdrawing chlorine enhances target affinity. This compound serves as a key intermediate in medicinal chemistry for developing antiviral and anticancer agents.
4-Chloro-6-phenylpyrimidin-2-amine serves as a versatile building block in medicinal chemistry, enabling the construction of pyrimidine-based scaffolds prevalent in kinase inhibitors and antiviral agents. Its ortho-chloro functionality facilitates palladium-catalyzed cross-coupling reactions, while the primary amine supports derivatization via acylation or alkylation. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis campaigns in drug discovery workflows.
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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-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: