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Structure of 61500-87-6
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Methyl 2-amino-4-(trifluoromethyl)benzoate features a trifluoromethyl group enhancing electron-withdrawal and metabolic stability, paired with a primary amine enabling direct derivatization. This bench-stable, moisture-tolerant ester integrates readily into pharmaceutical intermediates and functional materials synthesis under standard conditions.
Methyl 2-amino-4-(trifluoromethyl)benzoate serves as a versatile building block in medicinal chemistry, enabling the synthesis of biologically active heterocycles and pharmaceutical intermediates. Its ortho-amino and trifluoromethyl groups provide complementary reactivity for electrophilic substitution, coupling reactions, and cyclization processes. The methyl ester functionality offers ease of manipulation and purification, while the molecule exhibits good bench stability and functional group tolerance in standard synthetic 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: