756500-63-7

Basic information

• Product Name: 2-amino-3-(m-chlorophenyl)-1,8-naphthyridine
• Synonyms: 2-amino-3-(m-chlorophenyl)-1,8-naphthyridine
• CAS NO: 756500-63-7
• Molecular Weight: 255.707
• Mol File: 756500-63-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-amino-3-(m-chlorophenyl)-1,8-naphthyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-3-(m-chlorophenyl)-1,8-naphthyridine(756500-63-7)
• EPA Substance Registry System: 2-amino-3-(m-chlorophenyl)-1,8-naphthyridine(756500-63-7)

Safety Data

• Hazardous Substances Data: 756500-63-7(Hazardous Substances Data)

Upstream product

• 7521-41-7 2-Aminonicotinaldehyde 
• 1529-41-5 3-chloro-benzeneacetonitrile 

Downstream Products

• 1312026-94-0 C₂₂H₂₀ClN₃O 
• 756500-74-0 N-benzo[1,3]dioxol-5-ylmethylene-N'-[3-(3-chloro-phenyl)-[1,8]naphthyridin-2-yl]-hydrazine 
• 756500-72-8 N-[3-(3-Chloro-phenyl)-[1,8]naphthyridin-2-yl]-N'-[1-(3-nitro-phenyl)-meth-(Z)-ylidene]-hydrazine 
• 756500-73-9 N-[3-(3-Chloro-phenyl)-[1,8]naphthyridin-2-yl]-N'-[1-(4-nitro-phenyl)-meth-(Z)-ylidene]-hydrazine 
• 756500-67-1 N-[3-(3-Chloro-phenyl)-[1,8]naphthyridin-2-yl]-N'-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-hydrazine 
• 756500-71-7 N-[1-(2-Bromo-phenyl)-meth-(Z)-ylidene]-N'-[3-(3-chloro-phenyl)-[1,8]naphthyridin-2-yl]-hydrazine 
• 756500-68-2 N-[3-(3-chloro-phenyl)-[1,8]naphthyridin-2-yl]-N'-(4-methyl-benzylidene)-hydrazine 
• 756500-69-3 N-[1-(2-Chloro-phenyl)-meth-(Z)-ylidene]-N'-[3-(3-chloro-phenyl)-[1,8]naphthyridin-2-yl]-hydrazine 
• 756500-70-6 N-[1-(4-Chloro-phenyl)-meth-(Z)-ylidene]-N'-[3-(3-chloro-phenyl)-[1,8]naphthyridin-2-yl]-hydrazine 
• 756500-66-0 N-[3-(3-Chloro-phenyl)-[1,8]naphthyridin-2-yl]-N'-[1-phenyl-meth-(Z)-ylidene]-hydrazine 
• 519153-79-8 2-hydrazino-3-(m-chlorophenyl)-1,8-naphthyridine 
• 756500-65-9 2-chloro-3-(m-chlorophenyl)-1,8-naphthyridine 

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