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Structure of 854538-94-6
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2-Amino-3-fluorobenzaldehyde features a strategically positioned fluorine atom and amino group on the benzene ring, enabling selective coupling reactions in medicinal chemistry. This electron-rich scaffold integrates readily into heterocyclic systems, delivering enhanced solubility and metabolic stability in bioactive molecule synthesis under standard conditions.
2-Amino-3-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted benzimidazoles, quinoline derivatives, and other nitrogen-containing heterocycles. Its ortho-amino and aldehyde functionalities facilitate sequential coupling reactions and cyclizations under mild conditions, while the fluorine substituent enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by recrystallization, it functions effectively in standard amide, imine, and Ullmann-type transformations.
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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: