68289-19-0

Basic information

• Product Name: Ethanedione, bis[4-(diethylamino)phenyl]-
• CAS NO: 68289-19-0
• Molecular Formula: C22H28N2O2
• Molecular Weight: 352.477
• Mol File: 68289-19-0.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Ethanedione, bis[4-(diethylamino)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanedione, bis[4-(diethylamino)phenyl]-(68289-19-0)
• EPA Substance Registry System: Ethanedione, bis[4-(diethylamino)phenyl]-(68289-19-0)

Safety Data

• Hazardous Substances Data: 68289-19-0(Hazardous Substances Data)

Upstream product

• 306990-96-5 1H-1,2,3-benzotriazol-1-yl(4-diethylaminophenyl)-1,2-ethanedione 
• 579-39-5 1,2-bis(4-fluorophenyl)ethane-1,2-dione 
• 109-89-7 diethylamine 
• 79-37-8 oxalyl dichloride 
• 91-66-7 N,N-diethylaniline 

Downstream Products

• 57806-84-5 1,2-Bis<4,4'-N,N-diethylamino-phenyl>-1-hydroxy-ethan-2-on 

Relevant articles and documents

Pyrazino-[2,3-f][1,10]phenanthroline as a new anchoring group of organic dyes for dye-sensitized solar cells

Two novel donor-acceptor organic dyes (PPL-1 and PPL-2) with pyrazino-[2,3-f][1,10]phenanthroline as an electron-withdrawing anchoring group were designed and synthesized for dye-sensitized solar cells, achieving a promising power conversion efficiency of

Organic photosensitizer on basis of pyrazine [2,3-g] quinoxaline, method for preparing organic photosensitizer and photodynamic application thereof

The invention provides a photosensitizer. The photosensitizer comprises compounds on the basis of pyrazine [2,3-g] quinoxaline structural units. The photosensitizer has the advantages that the photosensitizer has the structural features of intramolecular

Samarium diiodide promoted formation of 1,2-diketones and 1-acylamido-2-substituted benzimidazoles from N-acylbenzotriazoles

N-Acylbenzotriazoles, when treated with samarium diiodide in THF, undergo self-coupling reaction to afford 1,2-diketones in good to excellent yields; while when treated with samarium diiodide in CH3CN, they undergo ring-opening reaction to afford 1-acylamido-2-alkyl (or aryl) benzimidazoles in reasonable to good yields. A plausible mechanism was suggested.