1451790-67-2

Basic information

• Product Name: N-(bis(4-tert-butylphenyl)methyl)-4-nitroaniline
• CAS NO: 1451790-67-2
• Molecular Weight: 416.563
• Mol File: 1451790-67-2.mol

Chemical Properties

• CAS DataBase Reference: N-(bis(4-tert-butylphenyl)methyl)-4-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-(bis(4-tert-butylphenyl)methyl)-4-nitroaniline(1451790-67-2)
• EPA Substance Registry System: N-(bis(4-tert-butylphenyl)methyl)-4-nitroaniline(1451790-67-2)

Safety Data

• Hazardous Substances Data: 1451790-67-2(Hazardous Substances Data)

Upstream product

• 274258-85-4 4-(benzhydrylamino)benzonitrile 
• 60999-93-1 2-benzhydryl-1,3-diphenylpropane-1,3-dione 
• 1451790-23-0 2-(bis(4-tert-butylphenyl)methyl)-1,3-diphenylpropane-1,3-dione 
• 100-01-6 4-nitro-aniline 
• 101-81-5 Diphenylmethane 

Relevant articles and documents

Iron-catalyzed C-C bond cleavage and C-N bond formation

A novel approach for C-N bond formation was developed by iron-catalyzed C-C bond cleavage. Anilines and sulfonamides reacted smoothly with 2-substituted 1,3-diphenylpropane-1,3-diones to afford N-alkylation products, in which the 1,3-dicarbonyl group acts as a leaving group in the presence of an iron catalyst. The reversible C-C bond cleavage plays a driving force to give the thermodynamically stable products. The method is complementary to the previous methods for C-N bond formation. Copyright