656250-04-3

Basic information

• Product Name: 5,6-DIHYDRO-9,10-DIMETHOXYBENZ[C]ACRIDINE
• Synonyms: 5,6-DIHYDRO-9,10-DIMETHOXYBENZ[C]ACRIDINE
• CAS NO: 656250-04-3
• Molecular Formula: C19H17NO2
• Molecular Weight: 291.34
• Mol File: 656250-04-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5,6-DIHYDRO-9,10-DIMETHOXYBENZ[C]ACRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 5,6-DIHYDRO-9,10-DIMETHOXYBENZ[C]ACRIDINE(656250-04-3)
• EPA Substance Registry System: 5,6-DIHYDRO-9,10-DIMETHOXYBENZ[C]ACRIDINE(656250-04-3)

Safety Data

• Hazardous Substances Data: 656250-04-3(Hazardous Substances Data)

Upstream product

• 1016-58-6 6-nitroveratryl alcohol 
• 529-33-9 1,2,3,4-Tetrahydro-1-naphthol 

Relevant articles and documents

Convenient synthesis of quinolines from α-2-nitroaryl alcohols and alcohols via a ruthenium-catalyzed hydrogen transfer strategy

A new and straightforward method for convenient synthesis of quinolines via a ruthenium-catalyzed hydrogen-transfer strategy has been demonstrated. By employing a commercially available ruthenium catalyst system, different α-2-nitroaryl alcohols were efficiently converted in combination with a variety of alcohols into various substituted products in reasonable to good yields upon isolation. The synthetic protocol is operationally simple with a broad substrate scope, and there is no need for the use of specialized reducing agents, making it a practical approach for versatile preparation of various quinoline derivatives.

A novel reductive cyclisation of o-nitrochalcones promoted by low-valent titanium: An access to 2-arylquinolines and 5,6-dihydrobenz[c]acridines

The intramolecular reductive cyclizations of o-nitrochalcones(1) induced by the TiCl4/Zn system were studied; 2-arylquinolines(2) and 5,6-dihydrobenz[c]acridines(4) were obtained in reasonable yields at room temperature conditions.