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Structure of 915087-25-1
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4-Amino-2-fluoro-N-methylbenzamide features a strategically positioned para-amino group and ortho-fluoro substituent on a benzamide scaffold, enabling selective coupling reactions in medicinal chemistry. The N-methyl substitution enhances metabolic stability while maintaining solubility under standard conditions. This compound serves as a key intermediate for bioactive molecule synthesis.
4-Amino-2-fluoro-N-methylbenzamide serves as a versatile building block in medicinal chemistry, enabling direct incorporation of both amino and fluoro functionalities into target molecules. Its N-methyl amide group enhances metabolic stability and modulates lipophilicity, while the ortho-fluoro substituent facilitates directed ortho-metalation and influences electronic properties. The compound exhibits excellent bench stability and is compatible with standard coupling reactions, simplifying access to complex heterocyclic scaffolds 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: