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2,4-Octadienoic acid, 4-ethyl-

Base Information
  • Chemical Name:2,4-Octadienoic acid, 4-ethyl-
  • CAS No.:72928-47-3
  • Molecular Formula:C10H16 O2
  • Molecular Weight:168.236
  • Hs Code.:
  • European Community (EC) Number:277-076-9
  • DSSTox Substance ID:DTXSID2072671
  • Nikkaji Number:J296.412K
  • Wikidata:Q76386864
  • Mol file:72928-47-3.mol
2,4-Octadienoic acid, 4-ethyl-

Synonyms:2,4-Octadienoic acid, 4-ethyl-;72928-47-3;4-Ethyl-2,4-octadienoic acid;4-Ethylocta-2,4-dienoic acid;(2E,4E)-4-ethylocta-2,4-dienoic acid;EINECS 277-076-9;DTXSID2072671;SCHEMBL13347104

Suppliers and Price of 2,4-Octadienoic acid, 4-ethyl-
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 8 raw suppliers
Chemical Property of 2,4-Octadienoic acid, 4-ethyl-
Chemical Property:
  • Vapor Pressure:0.000499mmHg at 25°C 
  • Boiling Point:291°C at 760 mmHg 
  • Flash Point:196.9°C 
  • PSA:37.30000 
  • Density:0.959g/cm3 
  • LogP:2.76370 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:168.115029749
  • Heavy Atom Count:12
  • Complexity:190
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCCC=C(CC)C=CC(=O)O
  • Isomeric SMILES:CCC/C=C(\CC)/C=C/C(=O)O
Technology Process of 2,4-Octadienoic acid, 4-ethyl-

There total 1 articles about 2,4-Octadienoic acid, 4-ethyl- 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 piperidine; pyridine;
upstream raw materials:

2-ethylhexenal

malonic acid

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