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Structure of 29874-83-7
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2-Chloro-4-phenylquinazoline delivers a robust heterocyclic scaffold for medicinal chemistry, featuring a chlorine atom at the C2 position and a phenyl group at C4. This substitution pattern enhances metabolic stability and facilitates targeted interactions in kinase inhibition studies. The compound exhibits excellent bench stability and solubility in common organic solvents, enabling seamless integration into synthetic workflows.
2-Chloro-4-phenylquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinazoline-based scaffolds through palladium-catalyzed cross-coupling reactions. Its chlorine substituent at the 2-position provides high reactivity in Suzuki-Miyaura and Buchwald-Hartwig couplings, facilitating rapid diversification of the core structure. The phenyl group at C4 enhances planarity and π-stacking potential, contributing to favorable binding interactions in kinase inhibitor design. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses of targeted pharmaceutical candidates.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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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: