113689-23-9

Basic information

• Product Name: C₃₁H₃₀N₂O₄S
• Synonyms: C₃₁H₃₀N₂O₄S
• CAS NO: 113689-23-9
• Molecular Weight: 526.656
• Mol File: 113689-23-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: C₃₁H₃₀N₂O₄S(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₁H₃₀N₂O₄S(113689-23-9)
• EPA Substance Registry System: C₃₁H₃₀N₂O₄S(113689-23-9)

Safety Data

• Hazardous Substances Data: 113689-23-9(Hazardous Substances Data)

Upstream product

• 113352-69-5 C₃₁H₃₂N₂O₄S 
• 96-96-8 4-methoxy-2-nitroaniline 
• 113352-69-5 C₃₁H₃₂N₂O₄S 
• 113352-68-4 (E)-1-carbomethoxy-2-methyl-6-methoxy-3-formimidoyl>indole 
• 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 
• 113352-70-8 C₃₁H₃₂N₂O₅S 
• 113352-70-8 C₃₁H₃₂N₂O₅S 

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