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Structure of 21575-13-3
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6,7-Dimethoxyquinazolin-4-amine delivers a potent heterocyclic scaffold with enhanced solubility and metabolic stability. The dimethoxy substitution pattern at the 6,7-positions confers favorable electronic properties for kinase inhibition, while the amine functionality enables direct coupling in medicinal chemistry campaigns. This bench-stable compound integrates efficiently into targeted drug discovery pipelines.
6,7-Dimethoxyquinazolin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to quinazoline-based kinase inhibitors and bioactive heterocycles. Its dimethoxy substitution pattern enhances solubility and modulates electronic properties, while the primary amine facilitates straightforward derivatization via amidation, alkylation, or coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in standard synthetic workflows for API development and scaffold diversification.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: