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Structure of 24101-09-5
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This trifluoromethyl-substituted pyrimidine amine features a reactive amine handle and electron-deficient heterocyclic core, enabling efficient coupling in cross-coupling and Heterocycle functionalization. The chloro group facilitates nucleophilic substitution under mild conditions, while the trifluoromethyl moiety imparts enhanced metabolic stability and lipophilicity.
2-Chloro-5-(trifluoromethyl)pyrimidin-4-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the amine functionality offers direct coupling potential. Its stability under standard bench conditions and compatibility with diverse functional groups make it well-suited for modular synthesis of bioactive compounds and API intermediates.
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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: