60859-72-5

Basic information

• Product Name: ethyl 2-nitro-3-(p-tolyl)acrylate
• Synonyms: ethyl 2-nitro-3-(p-tolyl)acrylate
• CAS NO: 60859-72-5
• Molecular Weight: 235.24
• Mol File: 60859-72-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl 2-nitro-3-(p-tolyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-nitro-3-(p-tolyl)acrylate(60859-72-5)
• EPA Substance Registry System: ethyl 2-nitro-3-(p-tolyl)acrylate(60859-72-5)

Safety Data

• Hazardous Substances Data: 60859-72-5(Hazardous Substances Data)

Upstream product

• 626-35-7 nitroacetic acid ethyl ester 
• 104-87-0 4-methyl-benzaldehyde 
• 60859-79-2 (Z)-ethyl 2-nitro-3-(p-tolyl)acrylate 
• 2362-77-8 (4-methylbenzylidene)phenylamine 
• 20511-20-0 ethyl p-methylcinnamate 

Downstream Products

• 1206899-37-7 C₁₅H₁₈N₂O₆ 
• 1206899-34-4 ethyl 3-(4-methylphenyl)-2-nitro-3-N-(phthalimido)propanoate 
• 99484-07-8 N-((4-methylphenyl)methylene)-1-propanamine 
• 21758-00-9 ethyl 3-(p-tolyl)pent-2-enoate 

Relevant articles and documents

Catalytic Enantioselective Synthesis of 3,4,5-Trisubstituted Isoxazoline N-Oxides and Regioselective Synthesis of 3,4,5-Trisubstituted Isoxazoles

An efficient catalytic asymmetric synthesis of 3,4,5-trisubstituted isoxazoline N-oxides and regioselective synthesis of 3,4,5-trisubstituted isoxazoles has been described. α-Nitrocinnamates and α-nitrobenzophenones were utilized as Michael acceptors resp

Nucleophilic addition to nitroacrylates: application towards the synthesis of 2,3-dehydroamino acids and 2,3-diamino acids

The addition of the N-pronucleophiles to 2- or 3-nitro-2-alkenoates in the presence of base provided Michael addition products. In the case of 3-nitro compounds, reaction occurred via the formation of α-adducts and the subsequent elimination of nitrous ac