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Structure of 391-93-5
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Ethyl 2-amino-5-fluorobenzoate features a strategically positioned amino group flanked by electron-withdrawing fluorine and ester functionalities, enabling facile derivatization in medicinal chemistry. This bench-stable compound integrates readily into scaffold diversification campaigns, particularly for targeting kinase inhibitors and CNS-active molecules.
Ethyl 2-amino-5-fluorobenzoate serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocycles and bioactive scaffolds. Its amino and ester functionalities offer orthogonal reactivity for sequential transformations, including amide coupling, electrophilic substitution, and transition-metal-catalyzed cross-coupling. The molecule exhibits good bench stability, facilitates straightforward purification, and functions reliably in standard synthetic workflows for 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-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: