95432-79-4

Basic information

• Product Name: N¹,N³-di(naphthalen-1-yl)propane-1,3-diamine
• Synonyms: N¹,N³-di(naphthalen-1-yl)propane-1,3-diamine
• CAS NO: 95432-79-4
• Molecular Weight: 326.441
• Mol File: 95432-79-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N¹,N³-di(naphthalen-1-yl)propane-1,3-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N¹,N³-di(naphthalen-1-yl)propane-1,3-diamine(95432-79-4)
• EPA Substance Registry System: N¹,N³-di(naphthalen-1-yl)propane-1,3-diamine(95432-79-4)

Safety Data

• Hazardous Substances Data: 95432-79-4(Hazardous Substances Data)

Upstream product

• 6628-35-9 3-(naphthalen-1-ylamino)propan-1-ol 
• 134-32-7 1-amino-naphthalene 

Downstream Products

• 230-27-3 7,8-benzoquinoline 
• 134-32-7 1-amino-naphthalene 

Relevant articles and documents

N-Heterocyclization of naphthylamines with 1,2- And 1,3-Diols catalyzed by an iridium Chloride/BINAP system

Benzoquinoline derivatives were successfully synthesized by iridium-catalyzed N-heterocyclization of naphthylamines with diols. For instance, the reaction of 1-naphthylamine with 1,3-propanediol catalyzed by IrCl3 combined with BINAP as a ligand produced 7,8-benzoquinoline in quantitative yield. The VV-heterocyclization reaction was found to be markedly influenced by the ligands employed. Benzoindoles were also synthesized by the same strategy from napthylamines with 1,2-diols. A reaction mechanism for the N-heterocyclization of naphthylamines with 1,3-diols by IrCl3 was proposed.