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Structure of 61948-59-2
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2,4-Dichloro-5-methoxyquinazoline features a sterically hindered quinazoline core with orthogonal halogen and methoxy substituents, enabling selective cross-coupling in late-stage functionalization. This bench-stable scaffold integrates readily into kinase inhibitor architectures and serves as a robust building block for targeted covalent probe development under standard conditions.
2,4-Dichloro-5-methoxyquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The dichloro substitution pattern facilitates sequential derivatization at C2 and C4 positions, while the methoxy group enhances solubility and modulates electronic properties. Its bench-stable nature and compatibility with diverse nucleophiles make it ideal for constructing quinazoline-based kinase inhibitors and other bioactive scaffolds.
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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: