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Structure of 367-31-7
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4-Fluorobenzene-1,2-diamine features a fluorinated aromatic ring with adjacent primary amine groups, enabling efficient coupling in pharmaceutical and agrochemical synthesis. The para-fluoro substitution enhances electronic effects and metabolic stability, while the diamine functionality offers dual sites for conjugation. This bench-stable compound integrates readily into complex molecular architectures under standard conditions.
4-Fluorobenzene-1,2-diamine serves as a versatile building block for the synthesis of heterocyclic scaffolds and functionalized arylamines. Its ortho-diamine motif enables efficient cyclization with carbonyl equivalents, facilitating access to substituted quinazolines and other nitrogen-containing heterocycles. The fluorine substituent enhances metabolic stability and modulates electronic properties, offering favorable reactivity in palladium-catalyzed cross-coupling processes. Bench-stable and readily purified by recrystallization, it functions reliably in both medicinal chemistry and process development workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: