1401520-03-3

Basic information

• Product Name: 3-(4-tert-butylphenyl)-5-nitro-4-p-tolyl-pentanoic acid methyl ester
• CAS NO: 1401520-03-3
• Molecular Weight: 383.488
• Mol File: 1401520-03-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(4-tert-butylphenyl)-5-nitro-4-p-tolyl-pentanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-tert-butylphenyl)-5-nitro-4-p-tolyl-pentanoic acid methyl ester(1401520-03-3)
• EPA Substance Registry System: 3-(4-tert-butylphenyl)-5-nitro-4-p-tolyl-pentanoic acid methyl ester(1401520-03-3)

Safety Data

• Hazardous Substances Data: 1401520-03-3(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 7559-36-6 4-methyl-β-nitrostyrene 
• 84434-23-1 3-(4-(tert-butyl)phenyl)acrylaldehyde 

Relevant articles and documents

N-heterocyclic carbene catalyzed homoenolate-addition reaction of enals and nitroalkenes: Asymmetric synthesis of 5-carbon-synthon δ-nitroesters

Synthesizing synthons: The highly enantioselective title reaction is described. It employs catalytic amounts of N-heterocyclic carbene precursors and transforms a broad range of nitroalkenes, such as nitrodienes, nitroenynes, and nitrostyrenes, through reaction with a broad range of enals, into δ-nitroesters via homoenolate intermediates (see scheme). Copyright