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2,4-Pentadienenitrile

Base Information Edit
  • Chemical Name:2,4-Pentadienenitrile
  • CAS No.:1615-70-9
  • Molecular Formula:C5H5 N
  • Molecular Weight:79.1014
  • Hs Code.:
  • European Community (EC) Number:216-566-9
  • DSSTox Substance ID:DTXSID8075099
  • Mol file:1615-70-9.mol
2,4-Pentadienenitrile

Synonyms:2,4-Pentadienenitrile;1615-70-9;C5-H5-N;1-cyanobuta-1,3-diene;DTXSID8075099

Suppliers and Price of 2,4-Pentadienenitrile
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
Total 6 raw suppliers
Chemical Property of 2,4-Pentadienenitrile Edit
Chemical Property:
  • Vapor Pressure:7.36mmHg at 25°C 
  • Melting Point:-60°C 
  • Refractive Index:1.4880 
  • Boiling Point:136.5°Cat760mmHg 
  • Flash Point:39.1°C 
  • PSA:23.79000 
  • Density:0.849g/cm3 
  • LogP:1.25218 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:79.042199164
  • Heavy Atom Count:6
  • Complexity:102
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Chemical Classes:Nitrogen Compounds -> Nitriles
  • Canonical SMILES:C=CC=CC#N
Technology Process of 2,4-Pentadienenitrile

There total 9 articles about 2,4-Pentadienenitrile 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 ethanolate; In ethanol; at 20 ℃;
Guidance literature:
Multi-step reaction with 5 steps
1: 40 percent / n-butyl-lithium / tetrahydrofuran / 1 h / -30 °C
2: 57 percent / thionyl chloride, pyridine / CH2Cl2 / 2 h / Heating
3: 99 percent / methanol / 16 h / Heating
4: 99 percent / H2O2 / ammonium molibdate / methanol
5: 1 M sodium ethoxide / ethanol / 20 °C
With pyridine; n-butyllithium; thionyl chloride; dihydrogen peroxide; sodium ethanolate; ammonium molibdate; In tetrahydrofuran; methanol; ethanol; dichloromethane;
Guidance literature:
Multi-step reaction with 6 steps
1: 74 percent / m-chloroperbenzoic acid / CHCl3 / 16 h / 20 °C
2: 40 percent / n-butyl-lithium / tetrahydrofuran / 1 h / -30 °C
3: 57 percent / thionyl chloride, pyridine / CH2Cl2 / 2 h / Heating
4: 99 percent / methanol / 16 h / Heating
5: 99 percent / H2O2 / ammonium molibdate / methanol
6: 1 M sodium ethoxide / ethanol / 20 °C
With pyridine; n-butyllithium; thionyl chloride; dihydrogen peroxide; sodium ethanolate; 3-chloro-benzenecarboperoxoic acid; ammonium molibdate; In tetrahydrofuran; methanol; ethanol; dichloromethane; chloroform;
Refernces Edit
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