60467-61-0

Basic information

• Product Name: 1,8-Naphthyridin-2-amine, 3-(4-fluorophenyl)-
• CAS NO: 60467-61-0
• Molecular Formula: C14H10FN3
• Molecular Weight: 239.252
• Mol File: 60467-61-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,8-Naphthyridin-2-amine, 3-(4-fluorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,8-Naphthyridin-2-amine, 3-(4-fluorophenyl)-(60467-61-0)
• EPA Substance Registry System: 1,8-Naphthyridin-2-amine, 3-(4-fluorophenyl)-(60467-61-0)

Safety Data

• Hazardous Substances Data: 60467-61-0(Hazardous Substances Data)

Upstream product

• 7521-41-7 2-Aminonicotinaldehyde 
• 459-22-3 4-fluorophenylacetonitrile 

Downstream Products

• 1153668-78-0 2-hydrazino-3-(4-fluorophenyl)-1,8-naphthyridine 
• 1345691-28-2 C₂₁H₁₅FN₄ 
• 1345691-29-3 C₂₂H₁₇FN₄ 
• 1233246-28-0 C₂₂H₁₂FN₃O₂ 
• 1082429-86-4 2-chloro-3-(4-fluorophenyl)-1,8-naphthyridine 
• 1082429-76-2 1,2-dihydro-3-(4-fluorophenyl)-1,8-naphthyridin-2-one 
• 1345691-43-1 C₂₃H₁₇FN₄O₂ 
• 1345691-42-0 C₂₁H₁₂FN₅O₂ 
• 1345691-41-9 C₂₁H₁₂FN₅O₂ 
• 1345691-40-8 C₂₁H₁₂ClFN₄ 
• 1345691-39-5 C₂₁H₁₂ClFN₄ 
• 1345691-38-4 C₂₂H₁₅FN₄O 
• 1345691-37-3 C₂₂H₁₅FN₄ 
• 1345691-36-2 C₂₁H₁₃FN₄ 

Relevant articles and documents

Green Synthesis of Fused Imidazo[1,2-a][1,8]naphthyridine Derivatives Catalyzed by DABCO under Solvent-Free Solid-State Conditions and Their Biological Evaluation

An efficient and eco-friendly methodology has been developed for the construction of fused imidazo[1,2-a][1,8]naphthyridine derivatives in the presence of 1,4-diazabicyclo[2.2.2]octane, and involving various substituted heterocyclic amines with phenacyl b

Green synthesis of 1,2,4-triazolo[4,3-a][1,8]naphthyridines using PhI(OAc)2-Al2O3 under microwave irradiation

Alumina-supported iodobenzene diacetate [PhI(OAc)2-Al 2O3] is a highly efficient reagent for the oxidative cyclization of N-arylidene-N′-[3-(4-fluorophenyl)-[1,8]naphthyridin-2-yl]- hy-drazines 7 to 1-aryl-4-[4-fluoro phenyl]-1,2,4-triazolo[4,3-a][1,8] naphthyridines 8 in solvent-free conditions under microwave irradiation. The products are obtained in good yields and excellent purities. The structural assignments of compounds 3-8 were based on their spectral (IR, 1H NMR and MS) and analytical data.