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Structure of 396-02-1
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2,4-Dichloro-7-(trifluoromethyl)quinazoline features a trifluoromethyl group that enhances metabolic stability and lipophilicity, while the dichloro substitution pattern supports targeted electrophilic functionalization. This quinazoline scaffold serves as a privileged core in kinase inhibitor design, enabling efficient integration into bioactive molecules under standard coupling conditions.
2,4-Dichloro-7-(trifluoromethyl)quinazoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of kinase inhibitors and heterocyclic scaffolds. The dichloro substitution pattern facilitates selective nucleophilic aromatic substitution, while the trifluoromethyl group enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with standard coupling reactions make it ideal for parallel synthesis campaigns and API development workflows.
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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: