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Structure of 14790-42-2
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4-Chloro-2-phenylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, offering a rigid, electron-deficient platform for drug discovery. This bench-stable compound integrates readily into kinase inhibitors and bioactive molecules, where its phenyl and chloro substituents enable precise spatial and electronic tuning.
4-Chloro-2-phenylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds through palladium-catalyzed cross-coupling reactions. Its chloro group exhibits high reactivity toward nucleophilic substitution and Suzuki-Miyaura coupling, facilitating rapid diversification. The phenyl substituent enhances stability and provides a rigid aromatic handle, improving metabolic resistance in target molecules. This compound functions reliably in standard synthetic workflows, offering excellent bench stability and straightforward purification—ideal for scalable synthesis 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-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: