Description

4-(2-Fluoro-4-nitrophenyl)morpholine (CAS No. 2689-39-6) is a high-purity fluorinated nitrophenyl morpholine derivative with the molecular formula C₁₀H₁₁FN₂O₃. This compound is a valuable synthetic intermediate for pharmaceutical and agrochemical research, featuring a morpholine ring conjugated to a fluoronitrophenyl group, which enhances its reactivity in nucleophilic substitution and coupling reactions. Its well-defined structure (IUPAC name: 4-(2-fluoro-4-nitrophenyl)morpholine) ensures consistent performance in organic synthesis, particularly in the development of bioactive molecules. Available in >98% purity (HPLC), it is supplied in sealed packaging under inert gas to maintain stability. Ideal for medicinal chemistry, material science, and cross-coupling reactions.

Properties

• CAS Number: 2689-39-6
• Complexity: 253
• IUPAC Name: 4-(2-fluoro-4-nitro-phenyl)morpholine
• InChI: InChI=1S/C10H11FN2O3/c11-9-7-8(13(14)15)1-2-10(9)12-3-5-16-6-4-12/h1-2,7H,3-6H2
• InChI Key: ZEQCFSSBZPZEFJ-UHFFFAOYSA-N
• Exact Mass: 226.07537038
• Molecular Formula: C10H11FN2O3
• Molecular Weight: 226.20
• SMILES: C1COCCN1C2=C(C=C(C=C2)[N+](=O)[O-])F
• Topological: 58.3
• Monoisotopic Mass: 226.07537038
• Synonyms: 4-(2-fluoro-4-nitrophenyl)morpholine, 2689-39-6, DTXSID60387723, DTXCID10338745, 4-(2-FLUORO-4-NITRO-PHENYL)-MORPHOLINE, Morpholine, 4-(2-fluoro-4-nitrophenyl)-, 3-fluoro-4-morpholinonitrobenzene, MFCD03138381, Cambridge id 6614516, SCHEMBL210786, 3Fluoro-4-morpholinonitrobenzene, ZEQCFSSBZPZEFJ-UHFFFAOYSA-N, 36R3KP66K8, 3-fluoro-4-morpholinyl nitrobenzene, 3-fluoro-4-morpholinyl-nitrobenzene, SBB025014, STK351957, 1-Fluoro-2-morpholino-5-nitrobenzene, AKOS005168040, AKOS015922545, N-(2-Fluoro-4-nitrophenyl)morpholine, 4-(2-fluoro-4-nitro-phenyl)morpholine, SY005339, ST45134676, SR-01000238859, SR-01000238859-1

Application

4-(2-Fluoro-4-nitrophenyl)morpholine is widely used as a key intermediate in the synthesis of pharmaceuticals, particularly for developing kinase inhibitors and antimicrobial agents. Its fluoronitrophenyl moiety enables selective functionalization in Pd-catalyzed cross-coupling reactions, making it valuable for constructing complex heterocycles. Researchers also employ it in material science to modify polymer backbones or as a precursor for fluorescent probes due to its electron-withdrawing properties.

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