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4-Dodecyloxybenzonitrile

Base Information
  • Chemical Name:4-Dodecyloxybenzonitrile
  • CAS No.:29147-92-0
  • Molecular Formula:C19H29 N O
  • Molecular Weight:287.445
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80372696
  • Nikkaji Number:J1.225.159I
  • Wikidata:Q82160545
  • Mol file:29147-92-0.mol
4-Dodecyloxybenzonitrile

Synonyms:4-DODECYLOXYBENZONITRILE;4-(dodecyloxy)benzonitrile;29147-92-0;SCHEMBL7849485;DTXSID80372696;STK365909;AKOS001483576

Suppliers and Price of 4-Dodecyloxybenzonitrile
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 5 raw suppliers
Chemical Property of 4-Dodecyloxybenzonitrile
Chemical Property:
  • PSA:33.02000 
  • LogP:5.85798 
  • XLogP3:7.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:12
  • Exact Mass:287.224914549
  • Heavy Atom Count:21
  • Complexity:273
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCOC1=CC=C(C=C1)C#N
Technology Process of 4-Dodecyloxybenzonitrile

There total 4 articles about 4-Dodecyloxybenzonitrile 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 potassium carbonate; In butanone; for 24h; Reflux;
DOI:10.1016/j.tet.2011.10.019
Guidance literature:
With potassium carbonate; In butanone; Reflux;
DOI:10.1039/c4tc00886c
Guidance literature:
With potassium carbonate; In N,N-dimethyl-formamide; at 50 ℃; for 14h; Title compound not separated from byproducts.;
DOI:10.1021/jo702495u
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