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Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)-

Base Information
  • Chemical Name:Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)-
  • CAS No.:54744-68-2
  • Molecular Formula:C15H16N2O6
  • Molecular Weight:320.2973
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70203203
  • Wikidata:Q83076553
Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)-

Synonyms:BRN 0448351;Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)-;(Acetylamino)((5-methoxy-1H-indol-3-yl)methyl)propanedioic acid;54744-68-2;DTXSID70203203;LS-120057

Suppliers and Price of Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Total 0 raw suppliers
Chemical Property of Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)-
Chemical Property:
  • Vapor Pressure:1.96E-19mmHg at 25°C 
  • Boiling Point:680.2°Cat760mmHg 
  • Flash Point:365.2°C 
  • Density:1.456g/cm3 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:6
  • Exact Mass:320.10083623
  • Heavy Atom Count:23
  • Complexity:480
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)NC(CC1=CNC2=C1C=C(C=C2)OC)(C(=O)O)C(=O)O
Technology Process of Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)-

There total 3 articles about Propanedioic acid, (acetylamino)((5-methoxy-1H-indol-3-yl)methyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium hydroxide; In water; at 3 ℃; Reflux;
Guidance literature:
Multi-step reaction with 3 steps
1: acetic acid / water / 10 - 30 °C
2: sodium hydroxide / toluene / 18 h / Reflux
3: sodium hydroxide / water / 3 °C / Reflux
With acetic acid; sodium hydroxide; In water; toluene;
Guidance literature:
Multi-step reaction with 2 steps
1: sodium hydroxide / toluene / 18 h / Reflux
2: sodium hydroxide / water / 3 °C / Reflux
With sodium hydroxide; In water; toluene;
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