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Structure of 124429-27-2
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4-Chloro-8-fluoroquinazoline features a fused bicyclic core with strategically positioned halogen substituents, enabling direct functionalization in late-stage synthesis. The electron-deficient quinazoline scaffold facilitates efficient coupling reactions, while the ortho-halogen arrangement enhances regioselectivity in cross-coupling transformations under standard conditions. This compound serves as a key building block for bioactive heterocycles.
4-Chloro-8-fluoroquinazoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at C4 and C8 positions via palladium-catalyzed cross-coupling reactions. Its dual halogenation pattern supports sequential derivatization, while the electron-deficient quinazoline core enhances reactivity in nucleophilic substitution and transition-metal-catalyzed transformations. Bench-stable and compatible with standard purification methods, it facilitates efficient access to diverse heterocyclic scaffolds relevant to kinase inhibitor development.
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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: