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Structure of 78052-20-7
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2,4-Dichloro-5-methylquinazoline serves as a key heterocyclic scaffold in medicinal chemistry, featuring two chlorine substituents at electron-deficient positions and a methyl group at the 5-position. This combination enhances reactivity in nucleophilic substitution processes, enabling efficient coupling for pharmaceutical intermediates. The molecule exhibits good stability under standard bench conditions and facilitates rapid diversification in drug discovery campaigns.
2,4-Dichloro-5-methylquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The dichloro substitution pattern provides orthogonal reactivity for sequential derivatization, while the methyl group enhances solubility and modulates electronic properties. Bench-stable and readily purified by column chromatography, it functions as a key scaffold for constructing kinase inhibitor libraries 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: