1382847-03-1

Basic information

• Product Name: N-(2,4-dimethylphenyl)-N-methylmethacrylamide
• Synonyms: N-(2,4-dimethylphenyl)-N-methylmethacrylamide
• CAS NO: 1382847-03-1
• Molecular Weight: 203.284
• Mol File: 1382847-03-1.mol

Chemical Properties

• CAS DataBase Reference: N-(2,4-dimethylphenyl)-N-methylmethacrylamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,4-dimethylphenyl)-N-methylmethacrylamide(1382847-03-1)
• EPA Substance Registry System: N-(2,4-dimethylphenyl)-N-methylmethacrylamide(1382847-03-1)

Safety Data

• Hazardous Substances Data: 1382847-03-1(Hazardous Substances Data)

Upstream product

• 95-68-1 2,4-Xylidine 
• 29639-60-9 N-(2,4-dimethylphenyl)methacrylamide 
• 74-88-4 methyl iodide 

Relevant articles and documents

Synthesis of oxindoles via Cu-mediated reactions between N-phenylacrylamides and ethyl 2-bromo-2-methylpropionate

A novel way of synthesizing alkylated oxindoles via Cu-mediated atom transfer radical addition reaction between N-phenylacrylamides and ethyl 2-bromo-2-methylpropionate has been described. It was found that the use of N,N,N′,N′-1,1,2,2,-tetramethylethylenediamine as ligand was important for achieving good yields. Additionally, the use of DMSO as solvent and running the reaction at 130 °C were also crucial. In some cases, the product can be further brominated when the reaction temperature was raised to 150 °C.

Synthesis of Perfluoroalkyl-Substituted Oxindoles through Organophotoredox-Catalyzed Perfluoroalkylation of N-arylacrylamides with Perfluoroalkyl Iodides

An efficient process was developed for the perfluoroalkylation of N -arylacrylamides through an organocatalyzed photoredox/cyclization reaction of N -arylacrylamides with inexpensive perfluoroalkyl iodide reagents. The reaction employs an inexpensive organic dye, eosin Y, as the photoredox catalyst and is run under irradiation by a 26 W LED lightbulb.