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Structure of 6141-13-5
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2-Chloroquinazoline serves as a pivotal heterocyclic scaffold in medicinal chemistry, featuring a chlorine atom at the 2-position that enhances electrophilicity for nucleophilic substitution. This electron-deficient core integrates readily into kinase inhibitors and targeted therapeutics, offering high reactivity under standard conditions while maintaining bench-stable handling characteristics.
2-Chloroquinazoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C2 position via palladium-catalyzed cross-coupling reactions. Its electrophilic chlorine atom facilitates efficient substitution with amines, thiols, and arylborons, supporting rapid diversification of quinazoline scaffolds. The compound exhibits excellent bench stability and compatibility with common protecting groups, making it well-suited for modular synthesis of kinase inhibitors and other bioactive heterocycles.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H301-H318
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Precautionary Statements : P264-P270-P280-P405
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Lot numbers can be found on the outside label of a product: