1380315-89-8

Basic information

• Product Name: C₃₃H₄₂N₄O₆
• Synonyms: C₃₃H₄₂N₄O₆
• CAS NO: 1380315-89-8
• Molecular Weight: 590.72
• Mol File: 1380315-89-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₃H₄₂N₄O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₃H₄₂N₄O₆(1380315-89-8)
• EPA Substance Registry System: C₃₃H₄₂N₄O₆(1380315-89-8)

Safety Data

• Hazardous Substances Data: 1380315-89-8(Hazardous Substances Data)

Upstream product

• 476-34-6 isoindigo 
• 91-56-5 indole-2,3-dione 
• 1380315-86-5 (3R,3'R)-di-tert-butyl,3'-bis(2-(methoxycarbonylamino)ethyl)-2,2'-dioxo-3,3'-biindoline-1,1'-dicarboxylate 
• 1380315-87-6 (3R,3'R)-di-tert-butyl 3,3'-bis(2-nitroethyl)-2,2'-dioxo-3,3'-biindoline-1,1'-dicarboxylate 
• 1392467-98-9 C₂₈H₃₁N₃O₈ 
• 1380315-88-7 di-tert-butyl 2,2′-dioxo-[3,3′-biindoline]-1,1′-dicarboxylate 

Downstream Products

• 595-05-1 (4bR,5S,10bR,11S)-13,18-dimethyl-5,6,11,12-tetrahydro-5,10b:11,4b-bis(epiminoethano)dibenzo[c,h][2,6]naphthyridine 

Relevant articles and documents

Catalytic asymmetric total synthesis of chimonanthine, folicanthine, and calycanthine through double michael reaction of bisoxindole

Direct access: Sterically hindered vicinal quaternary carbon stereocenters were constructed by catalytic enantio- and diastereoselective double Michael reaction, providing straightforward access to dimeric hexahydropyrroloindole alkaloids. A Mn(4-fluorobenzoate)2/Schiff base complex and a Mg(OAc)2/benzoic acid system were used as catalysts. Copyright