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Structure of 134517-55-8
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2,4,5-Trichloroquinazoline features a highly electron-deficient quinazoline core with three strategically positioned chlorine substituents. This configuration enhances reactivity in nucleophilic substitution processes and provides stability under standard bench conditions. The molecule serves as a key scaffold for synthesizing bioactive heterocycles in medicinal chemistry and materials science applications.
2,4,5-Trichloroquinazoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at multiple positions due to its electron-deficient heterocyclic core. The trichloro substitution pattern facilitates nucleophilic aromatic substitution (SNAr) under mild conditions, allowing efficient introduction of diverse amine and thiol derivatives. Its bench-stable nature and compatibility with common reaction protocols make it a practical choice for synthesizing kinase inhibitor scaffolds and other bioactive heterocycles.
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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: