41128-14-7

Basic information

• Product Name: 1-trityl-1H-indole-2,3-dione
• Synonyms: 1-trityl-1H-indole-2,3-dione
• CAS NO: 41128-14-7
• Molecular Weight: 389.453
• Mol File: 41128-14-7.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1-trityl-1H-indole-2,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-trityl-1H-indole-2,3-dione(41128-14-7)
• EPA Substance Registry System: 1-trityl-1H-indole-2,3-dione(41128-14-7)

Safety Data

• Hazardous Substances Data: 41128-14-7(Hazardous Substances Data)

Upstream product

• 596-43-0 bromo-triphenyl-methane 
• 91-56-5 indole-2,3-dione 
• 2206-53-3 trityl iodide 
• 76-83-5 trityl chloride 

Downstream Products

• 124382-90-7 1-trityl-indoline-2,3-dione-3-phenylhydrazone 
• 1263090-39-6 C₄₀H₂₉NO₄ 
• 1259382-69-8 (R)-benzyl 2-(3-hydroxy-2-oxo-1-tritylindolin-3-yl)acrylate 
• 1313872-24-0 C₃₈H₃₆N₂O₃S 
• 1313872-64-8 C₃₇H₃₄N₂O₂S 
• 1313872-65-9 C₃₇H₃₃BrN₂O₂S 
• 1313872-67-1 C₃₇H₃₃ClN₂O₂S 
• 1313872-69-3 C₃₉H₃₆N₂O₄S 
• 1313872-71-7 C₃₉H₃₇N₃O₃S 
• 1313872-73-9 C₃₉H₃₆N₂O₃S 
• 1403487-66-0 (2E,6E,NE)-1,8-diethoxy-1,8-dioxo-N-(2-oxo-1-tritylindolin-3-ylidene)octa-2,6-dien-4-amine oxide 
• 1403487-46-6 (E)-3-(hydroxyimino)-1-tritylindolin-2-one 
• 1403487-96-6 (E)-ethyl 3-[(E)-2-oxo-1-tritylindolin-3-ylideneaminooxy]but-2-enoate 

Relevant articles and documents

Applications of Ytterbium(II) Reagent as Grignard Reagent and Single-Electron Transfer Reagent in the Synthesis of 3-Substituted 2-Oxindoles

The use of ytterbium(II) reagent as both nucleophilic reagent and single-electron transfer reagent in the reaction of isatin derivatives with ytterbium(II) reagent is reported. From a synthetic point of view, a general, efficient, and experimentally simple one-pot method for the preparation of 3-substituted 2-oxindoles was developed.

Synthetic method of natural product (-)-Psychotriasine

The invention relates to a synthetic method of a natural product (-)-Psychotriasine. The method comprises the following steps of: using a compound of a known formula 1 as an initial raw material, carrying out a series of reactions such as triphenylmethyl

Enantioselective Rhodium-Catalyzed Addition of Arylboroxines to N-Unprotected Ketimines: Efficient Synthesis of Cipargamin

Highly enantioselective rhodium-catalyzed addition of arylboroxines to N-unprotected ketimines is realized for the first time by employing chiral BIBOP-type ligands with a Rh loading as low as 1 mol %. A range of chiral α-trifluoromethyl-α,α-diaryl α-tertiary amines or 3-amino-3-aryloxindoles were formed with excellent ee values and yields by employing either WingPhos or PFBO-BIBOP as the ligand. The method has enabled an efficient enantioselective synthesis of cipargamin.