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Structure of 179552-75-1
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N4-(3-Chloro-4-fluorophenyl)-7-methoxyquinazoline-4,6-diamine features a quinazoline core bearing a methoxy group at C7 and diamino substituents at C4 and C6. The para-chloro-fluoro aryl moiety enhances target affinity, while the electron-rich diamine system facilitates conjugation in kinase inhibitor scaffolds. This compound integrates readily into medicinal chemistry campaigns targeting ATP-binding domains.
N4-(3-Chloro-4-fluorophenyl)-7-methoxyquinazoline-4,6-diamine serves as a key intermediate in the synthesis of kinase inhibitors and other bioactive heterocycles. Its dual amine functionality enables facile coupling reactions, while the 3-chloro-4-fluorophenyl and methoxy substituents provide enhanced solubility and metabolic stability. The compound exhibits bench-stable handling and is compatible with standard peptide and amide coupling protocols.
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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: