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Amphotalide

Base Information Edit
  • Chemical Name:Amphotalide
  • CAS No.:1673-06-9
  • Molecular Formula:C19H20N2O3
  • Molecular Weight:324.379
  • Hs Code.:2925190090
  • European Community (EC) Number:216-809-9
  • UNII:95818EH730
  • DSSTox Substance ID:DTXSID50862731
  • Nikkaji Number:J7.552C
  • Wikidata:Q27271762
  • NCI Thesaurus Code:C73155
  • ChEMBL ID:CHEMBL94192
  • Mol file:1673-06-9.mol
Amphotalide

Synonyms:amphotalide;N(5-(4-aminophenoxy)pentyl)phthalimide

Suppliers and Price of Amphotalide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • AMPHOTALIDE 95.00%
  • 5MG
  • $ 497.50
Total 18 raw suppliers
Chemical Property of Amphotalide Edit
Chemical Property:
  • Vapor Pressure:3.22E-11mmHg at 25°C 
  • Melting Point:113.5 °C 
  • Refractive Index:1.619 
  • Boiling Point:527.6 °C at 760 mmHg 
  • Flash Point:272.9 °C 
  • PSA:72.63000 
  • Density:1.245 g/cm3 
  • LogP:3.63320 
  • XLogP3:3.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:7
  • Exact Mass:324.14739250
  • Heavy Atom Count:24
  • Complexity:422
Purity/Quality:

99%, *data from raw suppliers

AMPHOTALIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(=O)N(C2=O)CCCCCOC3=CC=C(C=C3)N
  • Therapeutic Function Antischistosomal
Technology Process of Amphotalide

There total 12 articles about Amphotalide 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:
Multi-step reaction with 2 steps
1: 85 percent / K2CO3 / acetonitrile / 24 h / Heating
2: H2 / Pd/C / toluene / 48 h / normal pressure
With hydrogen; potassium carbonate; palladium on activated charcoal; In toluene; acetonitrile;
DOI:10.1039/b405602g
Guidance literature:
With hydrogen; palladium on activated charcoal; In toluene; for 48h; normal pressure;
DOI:10.1039/b405602g
Guidance literature:
Multi-step reaction with 3 steps
1: 73 percent / K2CO3 / dimethylformamide / 72 h
2: 85 percent / K2CO3 / acetonitrile / 24 h / Heating
3: H2 / Pd/C / toluene / 48 h / normal pressure
With hydrogen; potassium carbonate; palladium on activated charcoal; In N,N-dimethyl-formamide; toluene; acetonitrile;
DOI:10.1039/b405602g
Refernces Edit
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