50774-57-7

Basic information

• Product Name: 4,4'-(1,2-Phenylenedicarbonyl)bis(N,N-dimethylaniline)
• Synonyms: 1,2-Bis(p-dimethylaminobenzoyl)benzene;4,4'-(1,2-Phenylenedicarbonyl)bis(N,N-dimethylaniline)
• CAS NO: 50774-57-7
• Molecular Formula: C₂₄H₂₄N₂O₂
• Molecular Weight: 372.46
• Mol File: 50774-57-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4,4'-(1,2-Phenylenedicarbonyl)bis(N,N-dimethylaniline)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-(1,2-Phenylenedicarbonyl)bis(N,N-dimethylaniline)(50774-57-7)
• EPA Substance Registry System: 4,4'-(1,2-Phenylenedicarbonyl)bis(N,N-dimethylaniline)(50774-57-7)

Safety Data

• Hazardous Substances Data: 50774-57-7(Hazardous Substances Data)

Upstream product

• 74317-52-5 4,4-bis-(p-dimethylaminophenyl)-3,4-dihydro-1(2H)-phthalazinone 
• 7353-91-5 4-dimethylaminophenylmagnesium bromide 
• 4122-56-9 methyl o-formylbenzoate 
• 857005-73-3 2-(4-dimethylamino-benzyl)-benzoic acid 
• 74415-33-1 3,3-bis-(p-dimethylaminophenyl)-N-aminophthalimidine 
• 76763-92-3 4,4-Bis-(4-dimethylamino-phenyl)-4H-phthalazin-1-one 
• 74415-34-2 7-dimethylamino-4b-(p-dimethylaminophenyl)benzazulen-10-one 
• 861531-75-1 4'-dimethylamino-2-(4-dimethylamino-benzyl)-benzophenone 
• 118-75-2 chloranil 
• 71-43-2 benzene 

Downstream Products

• 619-84-1 p-N,N-dimethylaminobenzoic acid 
• 861530-92-9 1,2-bis-(4-dimethylamino-α-hydroxy-benzyl)-benzene 
• 90523-93-6 1,4-bis-(4-dimethylamino-phenyl)-phthalazine 

Relevant articles and documents

Water-soluble 1,3-diarylisobenzoheteroles: Syntheses and characterization

Efficient synthetic route to water-soluble 1,3-diarylisobenzoheteroles, including isobenzofuran, isobenzothiophene, and isobenzoselenophene, was developed. Based on our one-pot synthetic method for diarylisobenzofurans, novel D-π-D and A-π-A types of diarylisobenzoheteroles became accessible, and they could be smoothly converted to the water-soluble isobenzoheteroles. The photophysical properties of newly prepared isobenzoheteroles are also evaluated.

Antarafacial role of an aromatic nucleus; a novel regiospecific [π4a + π2a] intramolecular cycloaddition of the ene-ketene with an aromatic ring

The thermally generated ene-ketene undergoes a facile and regiospecific intramolecular cycloaddition with N,N-dimethylaniline to result in the novel formation of the azulenone derivative via a norcaradiene intermediate.