944471-27-6

Basic information

• Product Name: ethyl 2-((tert-butoxycarbonyloxy)(4-nitrophenyl)methyl)acrylate
• Synonyms: ethyl 2-((tert-butoxycarbonyloxy)(4-nitrophenyl)methyl)acrylate
• CAS NO: 944471-27-6
• Molecular Weight: 351.356
• Mol File: 944471-27-6.mol

Chemical Properties

• CAS DataBase Reference: ethyl 2-((tert-butoxycarbonyloxy)(4-nitrophenyl)methyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-((tert-butoxycarbonyloxy)(4-nitrophenyl)methyl)acrylate(944471-27-6)
• EPA Substance Registry System: ethyl 2-((tert-butoxycarbonyloxy)(4-nitrophenyl)methyl)acrylate(944471-27-6)

Safety Data

• Hazardous Substances Data: 944471-27-6(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 88039-47-8 ethyl 2-(4-nitrohydroxybenzyl)acrylate 
• 555-16-8 4-nitrobenzaldehdye 
• 140-88-5 ethyl acrylate 

Downstream Products

• 1395055-52-3 C₂₈H₂₁NO₆ 
• 1395055-55-6 C₂₈H₂₇NO₆ 
• 1395055-34-1 C₂₈H₂₀N₂O₈ 
• 1412439-17-8 C₂₈H₂₀N₂O₈ 
• 1395055-54-5 C₂₈H₂₀BrNO₆ 
• 1395055-53-4 C₂₈H₂₀BrNO₆ 
• 1394249-79-6 (R)-methyl 4-(1-(ethoxycarbonyl)vinyl)-3,3-dicyano-2-(4-fluorophenyl)-4-(4-nitrophenyl)cyclopent-1-enecarboxylate 
• 1394249-78-5 (R)-methyl 4-(1-(ethoxycarbonyl)vinyl)-3,3-dicyano-4-(4-nitrophenyl)-2-p-tolylcyclopent-1-enecarboxylate 

Relevant articles and documents

Direct Synthesis of Dihydropyrrolo[2,1-a]Isoquinolines through FeCl3 Promoted Oxidative Aromatization

We have developed a straightforward FeCl3 promoted synthesis of dihydropyrrolo[2,1-a]isoquinolines through formal (3+2) cycloaddition/oxidative aromatization cascade of dihydroisoquinoline with Morita-Baylis-Hillman carbonates (up to 96% yield)

A highly regio- and stereo-selective [3+2] annulation of allylic compounds and 2-substituted 1,1-dicyanoalkenes through a catalytic carbon-phosphorus ylide reaction

A highly regio- and stereo-selective phosphine-catalyzed [3+2] annulation reaction between allylic compounds and 2-substituted 1,1-dicyanoalkenes through a catalytic phosphorus ylide reaction was developed. This reaction has the total reversed regioselect