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Structure of 74151-22-7
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4-Chloro-2-methyl-6-nitroquinazoline features a fused bicyclic core with electron-withdrawing nitro and chloro substituents positioned for enhanced reactivity in cross-coupling and medicinal chemistry applications. The methyl group at the 2-position provides steric control, while the para-nitro functionality enables facile derivatization. This compound serves as a key scaffold for kinase inhibitor development and exhibits favorable stability under standard bench conditions.
4-Chloro-2-methyl-6-nitroquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient access to kinase-inhibitor scaffolds. Its ortho-chloro and nitro groups facilitate palladium-catalyzed cross-coupling and selective reduction, while the methyl group enhances metabolic stability. The compound exhibits excellent bench stability and compatibility with standard purification protocols, making it well-suited for modular synthesis of bioactive quinazoline derivatives.
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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: