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Structure of 369-26-6
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Methyl 3-amino-4-fluorobenzoate features a strategically positioned amino group flanked by fluorine and ester functionalities, enabling selective coupling in medicinal chemistry. This electron-rich scaffold supports efficient derivatization under mild conditions, delivering key intermediates for bioactive compound synthesis.
Methyl 3-amino-4-fluorobenzoate serves as a versatile building block in medicinal chemistry, enabling efficient access to bioactive heterocycles and drug candidates. Its ortho-fluoro and amino functionalities facilitate directed metalation and electrophilic substitution, while the ester group supports selective transformations. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for multi-step synthesis workflows in 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: