1618671-09-2

Basic information

• Product Name: C₁₉H₁₄N₂O₃
• Synonyms: C₁₉H₁₄N₂O₃
• CAS NO: 1618671-09-2
• Molecular Weight: 318.332
• Mol File: 1618671-09-2.mol

Chemical Properties

• CAS DataBase Reference: C₁₉H₁₄N₂O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₉H₁₄N₂O₃(1618671-09-2)
• EPA Substance Registry System: C₁₉H₁₄N₂O₃(1618671-09-2)

Safety Data

• Hazardous Substances Data: 1618671-09-2(Hazardous Substances Data)

Upstream product

• 50899-39-3 N-methoxymethylisatin 
• 614-16-4 Benzoylacetonitrile 

Downstream Products

• 1618671-21-8 C₃₁H₂₅N₃O₇ 

Relevant articles and documents

Phosphine-catalyzed asymmetric [4+1] annulation of activated α,β-unsaturated ketones with Morita-Baylis-Hillman carbonates: Enantioselective synthesis of spirooxindoles containing two adjacent quaternary stereocenters

The asymmetric [4+1] annulation of activated α,β-unsaturated ketones with MBH carbonates catalyzed by bifunctional thiourea-phosphine catalysts derived from an axially chiral binaphthyl scaffold has been developed, giving spirooxindoles with two adjacent

Remote Asymmetric Oxa-Diels-Alder Reaction of 5-Allylic Furfurals via Dearomatizative Tetraenamine Catalysis

A previously unreported activation mode is developed through the generation of dearomatizative tetraenamine species between 5-allylic furfurals and a bifunctional amine-thiourea catalyst. The very remote ζ,η-alkenes perform as effective HOMO-raised dienophiles in inverse-electron-demand oxa-Diels-Alder cycloadditions with isatin-derived oxadiene substrates, delivering multifunctional spirocyclic oxindoles incorporating a dihydropyran skeleton in moderate to high yields with good to excellent enantio- and diastereoselectivity.