1169983-13-4

Basic information

• Product Name: methyl (1R,3S,3aR,6aS)-4,6-dioxo-3-(p-methylphenyl)-5-phenyl-octahydropyrrolo[3,4-c]pyrrole-1-carboxylate
• Synonyms: methyl (1R,3S,3aR,6aS)-4,6-dioxo-3-(p-methylphenyl)-5-phenyl-octahydropyrrolo[3,4-c]pyrrole-1-carboxylate
• CAS NO: 1169983-13-4
• Molecular Weight: 364.401
• Mol File: 1169983-13-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl (1R,3S,3aR,6aS)-4,6-dioxo-3-(p-methylphenyl)-5-phenyl-octahydropyrrolo[3,4-c]pyrrole-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (1R,3S,3aR,6aS)-4,6-dioxo-3-(p-methylphenyl)-5-phenyl-octahydropyrrolo[3,4-c]pyrrole-1-carboxylate(1169983-13-4)
• EPA Substance Registry System: methyl (1R,3S,3aR,6aS)-4,6-dioxo-3-(p-methylphenyl)-5-phenyl-octahydropyrrolo[3,4-c]pyrrole-1-carboxylate(1169983-13-4)

Safety Data

• Hazardous Substances Data: 1169983-13-4(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 104-87-0 4-methyl-benzaldehyde 
• 76862-10-7 (E)-[(4-methyl-benzylidene)-amino]-acetic acid methyl ester 

Relevant articles and documents

Development of chiral metal amides as highly reactive catalysts for asymmetric [3 + 2] cycloadditions

Highly efficient catalytic asymmetric [3 + 2] cycloadditions using a chiral copper amide are reported. Compared with the chiral CuOTf/Et3 N system, the CuHMDS system showed higher reactivity, and the desired reactions proceeded in high yields a

Highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides catalyzed by AgOAc/TF-BiphamPhos

A novel and highly efficient AgOAc/TF-BiphamPhos catalytic system shows excellent reactivity, diastereo-/enantioselectivity and structural scope in asymmetric 1,3-dipolar cycloaddition of azomethine ylides, especially derived from various α-substituted α-amino acids, with N-substituted maleimides and other electron-deficient alkenes.