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Structure of 6625-94-1
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2,4,7-Trichloroquinazoline features a highly electron-deficient quinazoline core with three chlorine substituents positioned to enhance reactivity in nucleophilic substitution processes. This structural configuration enables efficient coupling with diverse amines and heterocycles, making it a valuable scaffold for medicinal chemistry applications. The molecule exhibits robust stability under standard bench conditions and facilitates rapid derivatization without requiring harsh activation protocols.
2,4,7-Trichloroquinazoline serves as a versatile building block for the synthesis of biologically active heterocycles, enabling efficient construction of quinazoline-based scaffolds. Its three chlorine substituents provide orthogonal reactivity for nucleophilic substitution, facilitating the introduction of diverse aryl, alkyl, and amino groups under mild conditions. The compound exhibits excellent bench stability and is compatible with standard purification protocols, making it ideal for medicinal chemistry campaigns and process-scale applications.
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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: