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Allyl oct-2-enoate

Base Information
  • Chemical Name:Allyl oct-2-enoate
  • CAS No.:94135-94-1
  • Molecular Formula:C11H18O2
  • Molecular Weight:182.263
  • Hs Code.:
  • European Community (EC) Number:302-966-1
  • Nikkaji Number:J368.328A
  • Mol file:94135-94-1.mol
Allyl oct-2-enoate

Synonyms:Allyl oct-2-enoate;EINECS 302-966-1;94135-94-1;2-Octenoic acid 2-propenyl ester

Suppliers and Price of Allyl oct-2-enoate
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 4 raw suppliers
Chemical Property of Allyl oct-2-enoate
Chemical Property:
  • Vapor Pressure:0.0457mmHg at 25°C 
  • Boiling Point:237.1°Cat760mmHg 
  • Flash Point:98.3°C 
  • Density:0.9g/cm3 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:8
  • Exact Mass:182.130679813
  • Heavy Atom Count:13
  • Complexity:171
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCCCCC=CC(=O)OCC=C
  • Isomeric SMILES:CCCCC/C=C/C(=O)OCC=C
Technology Process of Allyl oct-2-enoate

There total 1 articles about Allyl oct-2-enoate 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 tris(dibenzylideneacetone)dipalladium(0) chloroform complex; formic acid; tributylphosphine; triethylamine; In tetrahydrofuran; at 40 ℃; for 2h; Mechanism; other alkynes;
DOI:10.1039/c39930000386
upstream raw materials:

allyl oct-2-ynoate

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