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2-Octadecenal

Base Information
  • Chemical Name:2-Octadecenal
  • CAS No.:56554-96-2
  • Molecular Formula:C18H34O
  • Molecular Weight:266.467
  • Hs Code.:
  • European Community (EC) Number:610-683-2
  • Nikkaji Number:J811.048D,J110.973A
  • Wikidata:Q76306613
  • Metabolomics Workbench ID:3625
2-Octadecenal

Synonyms:2-OCTADECENAL;(2E)-Octadecenal;(E)-octadec-2-enal;51534-37-3;E-2-Octadecenal;2E-Octadecenal;56554-96-2;(E)-2-OCTADECENAL;Koiganal I;2-Trans-octadecenal;SCHEMBL1302152;SCHEMBL1302154;(2E)-OCTADEC-2-ENAL;CHEBI:165518;LMFA06000232;AKOS015959074;E-2-Octadecenal CAS 51534-37-3

Suppliers and Price of 2-Octadecenal
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 3 raw suppliers
Chemical Property of 2-Octadecenal
Chemical Property:
  • Vapor Pressure:1.72E-05mmHg at 25°C 
  • Melting Point:33°C (estimate) 
  • Refractive Index:1.4688 (estimate) 
  • Boiling Point:364.1°C at 760 mmHg 
  • Flash Point:187.1°C 
  • PSA:17.07000 
  • Density:0.841g/cm3 
  • LogP:6.22280 
  • XLogP3:8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:15
  • Exact Mass:266.260965704
  • Heavy Atom Count:19
  • Complexity:196
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Chemical Classes:Other Classes -> Aldehydes
  • Canonical SMILES:CCCCCCCCCCCCCCCC=CC=O
  • Isomeric SMILES:CCCCCCCCCCCCCCC/C=C/C=O
Technology Process of 2-Octadecenal

There total 4 articles about 2-Octadecenal 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:

Reference yield: 89.0%

Guidance literature:
With manganese(IV) oxide; In tetrahydrofuran; n-heptane; at 0 - 20 ℃; for 3h; Time;
Guidance literature:
Multi-step reaction with 4 steps
1.1: n-butyllithium; N,N,N,N,N,N-hexamethylphosphoric triamide / tetrahydrofuran / 0.5 h / -78 °C / Inert atmosphere
1.2: 5 h / 20 °C / Inert atmosphere
2.1: toluene-4-sulfonic acid / methanol / 10 h / 20 °C
3.1: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / -10 - 50 °C / Inert atmosphere
4.1: manganese(IV) oxide / tetrahydrofuran; n-heptane / 3 h / 0 - 20 °C
With N,N,N,N,N,N-hexamethylphosphoric triamide; manganese(IV) oxide; lithium aluminium tetrahydride; n-butyllithium; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; n-heptane;
Guidance literature:
Multi-step reaction with 3 steps
1: toluene-4-sulfonic acid / methanol / 10 h / 20 °C
2: lithium aluminium tetrahydride / tetrahydrofuran / 4 h / -10 - 50 °C / Inert atmosphere
3: manganese(IV) oxide / tetrahydrofuran; n-heptane / 3 h / 0 - 20 °C
With manganese(IV) oxide; lithium aluminium tetrahydride; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; n-heptane;
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