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Phenylahistin

Base Information
  • Chemical Name:Phenylahistin
  • CAS No.:200815-37-8
  • Molecular Formula:C20H22N4O2
  • Molecular Weight:350.42
  • Hs Code.:
  • DSSTox Substance ID:DTXSID801336373
  • Nikkaji Number:J1.067.044F,J1.268.359F
  • Wikipedia:Phenylahistin
  • Wikidata:Q15425275
  • Metabolomics Workbench ID:103640
  • ChEMBL ID:CHEMBL319291
Phenylahistin

Synonyms:phenylahistin

Suppliers and Price of Phenylahistin
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
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of Phenylahistin
Chemical Property:
  • PSA:86.88000 
  • LogP:2.72910 
  • XLogP3:3
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:350.17427596
  • Heavy Atom Count:26
  • Complexity:593
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C=C)C1=C(N=CN1)C=C2C(=O)NC(C(=O)N2)CC3=CC=CC=C3
  • Isomeric SMILES:CC(C)(C=C)C1=C(N=CN1)/C=C\2/C(=O)N[C@H](C(=O)N2)CC3=CC=CC=C3
Technology Process of Phenylahistin

There total 3 articles about Phenylahistin 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:
C26H34N4O5; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;
With triethylamine; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/j.tetlet.2009.09.074
Guidance literature:
With triethylamine; In dichloromethane; at 20 ℃; for 2h;
Guidance literature:
With triethylamine; In dichloromethane; for 36h;
upstream raw materials:

C26H34N4O5

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