113370-91-5

Basic information

• Product Name: methyl 2-indol-3ylmethyl-4-p-nitrophenyl-6,8-dioxo-7-phenyl-3,7-diazabicyclo<3.3.0>octane-2-carboxylate
• CAS NO: 113370-91-5
• Molecular Weight: 524.533
• Mol File: 113370-91-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-indol-3ylmethyl-4-p-nitrophenyl-6,8-dioxo-7-phenyl-3,7-diazabicyclo<3.3.0>octane-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-indol-3ylmethyl-4-p-nitrophenyl-6,8-dioxo-7-phenyl-3,7-diazabicyclo<3.3.0>octane-2-carboxylate(113370-91-5)
• EPA Substance Registry System: methyl 2-indol-3ylmethyl-4-p-nitrophenyl-6,8-dioxo-7-phenyl-3,7-diazabicyclo<3.3.0>octane-2-carboxylate(113370-91-5)

Safety Data

• Hazardous Substances Data: 113370-91-5(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 113391-83-6 methyl N-p-nitrobenzylidenetryptophanate 
• 555-16-8 4-nitrobenzaldehdye 
• 6159-33-7 L-tryptophan hydrochloride 

Relevant articles and documents

X=Y-ZH Systems as Potential 1,3-Dipoles. Part 8. Pyrrolidines and Δ5-Pyrrolines (3,7-Diazabicyclooctenes) from the Reaction of Imines of α-Amino Acids and their Esters with Cyclic Dipolarophiles. Mechanism of Racemisation of α-Amino Acid

Imines of α-amino acid esters with aromatic, heterocyclic, and aliphatic aldehydes generate azomethine ylides stereospecifically by a prototropic shift on heating in toluene.The azomethine ylides undergo cycloaddition to N-phenylmaleimide, maleic anhydrid