99657-04-2

Basic information

• Product Name: C₃₀H₂₈N₂O₃S
• CAS NO: 99657-04-2
• Molecular Weight: 496.63
• Mol File: 99657-04-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₀H₂₈N₂O₃S(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₀H₂₈N₂O₃S(99657-04-2)
• EPA Substance Registry System: C₃₀H₂₈N₂O₃S(99657-04-2)

Safety Data

• Hazardous Substances Data: 99657-04-2(Hazardous Substances Data)

Upstream product

• 99657-01-9 (E)-1-carbomethoxy-2-methyl-3-indole 
• 99657-00-8 1-carbomethoxy-2-methyl-3-formylindole 
• 56232-16-7 (3R*,3aR*,4S*,7R*,7aS*)-3-hydroxy-3a,4,7,7a-tetrahydro-4,7-methanoisobenzofuran-1(3H)-one 
• 542-92-7 cyclopenta-1,3-diene 
• 98325-24-7 (1S,2R,3S,4R)-3-Vinyl-bicyclo[2.2.1]hept-5-ene-2-carbonyl chloride 
• 98325-25-8 (+/-)-(2,3-endo)-3-ethenylbicyclo<2.2.1>hept-5-ene-2-carboxylic acid 
• 5416-80-8 2-methyl-1H-indole-3-carbaldehyde 
• 99657-05-3 C₃₀H₃₀N₂O₄S 
• 99657-02-0 C₃₀H₃₀N₂O₃S 

Relevant articles and documents

Methods for Indole Alkaloid Synthesis: A Study of the Compatibility of the Indole-2,3-Quinodimethane Strategy for the Synthesis of 16-Methoxy-Substituted Aspidosperma-Type Alkaloids. Synthesis of (+)- and (-)-16-Methoxytabersonine

4-Methoxy-2-nitroaniline (5) is converted into 1-carbomethoxy-6-methoxy-3-formyl-2-methylindole (10) in an overall yield of 28percent through five steps.The derived imine from 10 and 2-(phenylthio)ethylamine on treatment with acid chloride (+/-)-12 gave h