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Structure of 721-09-5
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Methyl 3-amino-4-(trifluoromethoxy)benzoate features a trifluoromethoxy group that enhances metabolic stability and lipophilicity, while the para-amino functionality enables direct coupling in peptide and heterocyclic syntheses. This bench-stable derivative integrates readily into complex molecular architectures under standard conditions.
Methyl 3-amino-4-(trifluoromethoxy)benzoate serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. The amino group facilitates electrophilic substitution and coupling reactions, while the trifluoromethoxy moiety imparts enhanced metabolic stability and lipophilicity. Its bench-stable nature and compatibility with standard amide coupling and Suzuki-Miyaura protocols make it well-suited for scalable API development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: