1414941-81-3

Basic information

• Product Name: C₄₅H₃₅N₃O₄
• Synonyms: C₄₅H₃₅N₃O₄
• CAS NO: 1414941-81-3
• Molecular Weight: 681.791
• Mol File: 1414941-81-3.mol

Chemical Properties

• CAS DataBase Reference: C₄₅H₃₅N₃O₄(CAS DataBase Reference)
• NIST Chemistry Reference: C₄₅H₃₅N₃O₄(1414941-81-3)
• EPA Substance Registry System: C₄₅H₃₅N₃O₄(1414941-81-3)

Safety Data

• Hazardous Substances Data: 1414941-81-3(Hazardous Substances Data)

Upstream product

• 1215-59-4 5-benzyloxy-1H-indole 

Relevant articles and documents

Metal-free-catalyzed oxidative trimerization of indoles using NaNO 2 to construct quaternary carbon centers: Synthesis of 2-(1H-Indol-3-yl)-2,3′-biindolin-3-ones

A simple, convenient, and efficient synthesis of 2-(1H-indol-3-yl)-2, 3′-biindolin-3-one derivatives via a transition-metal-free-catalyzed oxidative trimeric reaction of indoles has been developed. This transformation may have occurred through a tandem oxidative homocoupling reaction by using NaNO2 in pyridine as oxidant. This methodology provides an alternative approach for the direct generation of all-carbon quaternary centers at the C2 position of indoles. Copyright

Copper-catalyzed oxidative trimerization of indoles by using TEMPO to construct quaternary carbon centers: The synthesis of 2-(1 H -indol-3-yl)-2,3′-biindolin-3-ones

A simple, convenient, and efficient synthesis of 2-(1H-indol-3-yl)-2, 3′-biindolin-3-one derivatives has been developed by the oxidative trimeric reaction of indoles using the TEMPO/CuCl2 catalyst system under ambient air. This methodology provides an alternative approach for the direct generation of all-carbon quaternary centers at the C-2 position of indoles.