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Structure of 16499-60-8
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4-Chloro-5-fluoroquinazoline features a fused bicyclic core with complementary halogen substituents enabling precise functionalization. The electron-deficient quinazoline scaffold supports efficient coupling reactions, while the ortho-halogen arrangement enhances reactivity in transition metal-catalyzed transformations. This bench-stable heterocycle serves as a key intermediate in medicinal chemistry for kinase inhibitor development and advanced synthetic routes.
4-Chloro-5-fluoroquinazoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C4 and C5 positions via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. Its dual halogenation pattern supports sequential derivatization, while the electron-deficient quinazoline core enhances reactivity in heterocyclic synthesis. Bench-stable and readily purified, it facilitates the construction of kinase inhibitor scaffolds and other bioactive heterocycles in scalable formats.
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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: