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Structure of 13036-50-5
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2-Chloro-4-phenylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorine substituent at the 2-position and a phenyl group at the 4-position. This arrangement imparts enhanced metabolic stability and facilitates efficient coupling in transition-metal-catalyzed reactions. The compound integrates readily into kinase inhibitor frameworks and other bioactive molecules.
2-Chloro-4-phenylpyrimidine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to construct biaryl and heteroaryl architectures. Its chlorine atom facilitates efficient functionalization under standard Suzuki-Miyaura and Buchwald-Hartwig conditions, while the phenyl-substituted pyrimidine core exhibits bench stability and compatibility with diverse reaction environments.
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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: