113352-80-0

Basic information

• Product Name: C₃₃H₃₄N₂O₆S
• Synonyms: C₃₃H₃₄N₂O₆S
• CAS NO: 113352-80-0
• Molecular Weight: 586.709
• Mol File: 113352-80-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₃H₃₄N₂O₆S(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₃H₃₄N₂O₆S(113352-80-0)
• EPA Substance Registry System: C₃₃H₃₄N₂O₆S(113352-80-0)

Safety Data

• Hazardous Substances Data: 113352-80-0(Hazardous Substances Data)

Upstream product

• 96-96-8 4-methoxy-2-nitroaniline 
• 113352-67-3 1-carbomethoxy-6-methoxy-3-formyl-2-methylindole 
• 113352-66-2 1-(4-methoxy-2-nitrophenyl)propan-2-one 
• 4147-43-7 6-methoxy-2-methylindole-3-carboxaldehyde 
• 1968-13-4 2-methyl-6-methoxy-1H-indole 
• 98325-24-7 (1S,2R,3S,4R)-3-Vinyl-bicyclo[2.2.1]hept-5-ene-2-carbonyl chloride 
• 113352-83-3 6-Methoxy-3-{[(E)-2-(2-methoxycarbonyl-phenylsulfanyl)-ethylimino]-methyl}-2-methyl-indole-1-carboxylic acid methyl ester 

Downstream Products

• 113352-87-7 C₃₃H₃₂N₂O₆S 

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