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Structure of 129112-65-8
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2,4-Dichloro-7-nitroquinazoline features a highly electron-deficient quinazoline core with dual chloro substituents at positions 2 and 4, enhancing reactivity for nucleophilic substitution. The para-nitro group at position 7 further increases electrophilicity, enabling efficient coupling in heterocyclic synthesis. This compound serves as a key scaffold for developing kinase inhibitors and advanced pharmaceutical intermediates under standard bench conditions.
2,4-Dichloro-7-nitroquinazoline serves as a versatile building block in medicinal chemistry, enabling regioselective functionalization at the C2 and C4 positions via palladium-catalyzed cross-coupling reactions. Its electron-deficient quinazoline core enhances reactivity in nucleophilic substitution processes, while the nitro group provides a handle for reduction and downstream derivatization. The compound exhibits good bench stability and facilitates the construction of complex heterocyclic scaffolds relevant to kinase inhibitor development.
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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: