79251-22-2

Basic information

• Product Name: 2-<(p-nitrophenoxy)carbonyl>benzyl-2',3'-dimethylimidazolium bromide
• Synonyms: 2-<(p-nitrophenoxy)carbonyl>benzyl-2',3'-dimethylimidazolium bromide
• CAS NO: 79251-22-2
• Molecular Weight: 432.274
• Mol File: 79251-22-2.mol

Chemical Properties

• CAS DataBase Reference: 2-<(p-nitrophenoxy)carbonyl>benzyl-2',3'-dimethylimidazolium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-<(p-nitrophenoxy)carbonyl>benzyl-2',3'-dimethylimidazolium bromide(79251-22-2)
• EPA Substance Registry System: 2-<(p-nitrophenoxy)carbonyl>benzyl-2',3'-dimethylimidazolium bromide(79251-22-2)

Safety Data

• Hazardous Substances Data: 79251-22-2(Hazardous Substances Data)

Upstream product

• 933-88-0 ortho-toluoyl chloride 
• 74738-56-0 4-nitrophenyl 2-methylbenzoate 
• 100-02-7 4-nitro-phenol 
• 1739-84-0 1,2-dimethyl-1H-imidazole 
• 79251-23-3 α-bromo-p-nitrophenyl o-toluate 

Downstream Products

• 14609-74-6 p-nitrophenolate 

Relevant articles and documents

Catalytic Mechanisms of Acyl Transfer Reactions in Dipolar Aprotic Media. 2. Electrophilic Activation of the Carbonyl Group by Quaternary Alkylammonium and Imidazolium Functions

Crown ether solvated potassium acetate in dipolar aprotic media readily converts p-nitrophenyl o-toluate to the corresponding acetyltoluyl mixed anhydride.The reaction proceeds at room temperature in quantitative yield.The rate of acyl transfer is 0.0118