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Structure of 124041-00-5
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4-Chloro-6-phenoxypyrimidine features a pyrimidine core with complementary electron-deficient and electron-rich substituents, enabling robust coupling reactions. The chlorine at C4 serves as a reliable electrophilic handle for palladium-catalyzed cross-couplings, while the phenoxypyrimidine scaffold imparts enhanced solubility and stability under standard conditions. This compound integrates efficiently into complex heterocyclic architectures.
4-Chloro-6-phenoxypyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group at C4 facilitates nucleophilic substitution reactions with amines, thiols, and other heteroatoms, while the phenoxypyrimidine core provides enhanced metabolic stability and favorable pharmacokinetic properties. This compound exhibits excellent bench stability and is readily purified by standard chromatographic methods, making it well-suited for scalable synthesis and high-throughput screening campaigns.
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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: