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Fendiline

Base Information
  • Chemical Name:Fendiline
  • CAS No.:13042-18-7
  • Molecular Formula:C23H25 N
  • Molecular Weight:351.919
  • Hs Code.:2921499090
  • European Community (EC) Number:235-915-6
  • UNII:S253D559A8
  • DSSTox Substance ID:DTXSID5048473
  • Nikkaji Number:J8.079I
  • Wikipedia:Fendiline
  • Wikidata:Q999767
  • NCI Thesaurus Code:C81686
  • Metabolomics Workbench ID:152054
  • ChEMBL ID:CHEMBL254832
  • Mol file:13042-18-7.mol
Fendiline

Synonyms:Fendilin;Fendiline;Fendiline Hydrochloride;Hydrochloride, Fendiline;Sensit;Senzit

Suppliers and Price of Fendiline
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
  • American Custom Chemicals Corporation
  • FENDILINE 95.00%
  • 5MG
  • $ 499.96
Total 8 raw suppliers
Chemical Property of Fendiline
Chemical Property:
  • Vapor Pressure:2.3E-08mmHg at 25°C 
  • Refractive Index:1.582 
  • Boiling Point:452.1°Cat760mmHg 
  • Flash Point:207.9°C 
  • PSA:12.03000 
  • Density:1.031g/cm3 
  • LogP:5.95030 
  • Water Solubility.:2.331mg/L(22.5 oC) 
  • XLogP3:5.5
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:7
  • Exact Mass:315.198699802
  • Heavy Atom Count:24
  • Complexity:303
Purity/Quality:

99% *data from raw suppliers

FENDILINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C1=CC=CC=C1)NCCC(C2=CC=CC=C2)C3=CC=CC=C3
  • Therapeutic Function Coronary vasodilator
Technology Process of Fendiline

There total 25 articles about Fendiline 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 trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 6h; Inert atmosphere;
DOI:10.1002/adsc.201701348
Guidance literature:
With potassium carbonate; In acetonitrile; at 80 ℃; for 20h;
DOI:10.1002/anie.201602130
Guidance literature:
With hydrogen; [Rh(1,3-dimesitylimidazole-2-ylidene)(cod)Cl]; In toluene; at 125 ℃; for 24h;
DOI:10.1002/chem.200601155
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