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2,6-Dimethoxy-4-vinylphenol

Base Information Edit
  • Chemical Name:2,6-Dimethoxy-4-vinylphenol
  • CAS No.:28343-22-8
  • Molecular Formula:C10H12 O3
  • Molecular Weight:180.203
  • Hs Code.:2909500000
  • European Community (EC) Number:848-947-6
  • UNII:ZB5OK5EX8B
  • DSSTox Substance ID:DTXSID30865427
  • Nikkaji Number:J588.629E
  • Wikipedia:Canolol
  • Wikidata:Q15634956
  • Mol file:28343-22-8.mol
2,6-Dimethoxy-4-vinylphenol

Synonyms:4-vinyl-2,6-dimethoxyphenol;canolol

Suppliers and Price of 2,6-Dimethoxy-4-vinylphenol
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
  • American Custom Chemicals Corporation
  • 2,6-DIMETHOXY-4-VINYLPHENOL 95.00%
  • 5MG
  • $ 499.02
Total 27 raw suppliers
Chemical Property of 2,6-Dimethoxy-4-vinylphenol Edit
Chemical Property:
  • Vapor Pressure:0.00163mmHg at 25°C 
  • Boiling Point:285.4°Cat760mmHg 
  • PKA:10.02±0.36(Predicted) 
  • Flash Point:126.4°C 
  • PSA:38.69000 
  • Density:1.113g/cm3 
  • LogP:2.05240 
  • XLogP3:2.3
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:180.078644241
  • Heavy Atom Count:13
  • Complexity:156
Purity/Quality:

99%, *data from raw suppliers

2,6-DIMETHOXY-4-VINYLPHENOL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC(=CC(=C1O)OC)C=C
  • Description Phenol, 4-ethenyl-2,6-dimethoxy- is an antioxidant phenolic compound that has potential use as a COX-2 inhibitor. It is also a flavoring agent and an antioxidant phenolic compound extracted from crude canola oil. It may inhibit tumor cell growth while inducing cell apoptosis.
  • Uses 4-Vinylsyringol is a useful antioxidant, antibacterial and antitumoral agent.
Technology Process of 2,6-Dimethoxy-4-vinylphenol

There total 17 articles about 2,6-Dimethoxy-4-vinylphenol 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:
ethyl(trisphenyl)phosphonium bromide; With potassium-t-butoxide; In tetrahydrofuran; at 20 ℃; for 0.5h; Inert atmosphere; Sealed tube;
syringic aldehyde; In tetrahydrofuran; at 0 - 20 ℃; for 40h; Inert atmosphere; Sealed tube;
DOI:10.1021/acs.orglett.2c00566
Guidance literature:
With Cocos nucifera juice; at 20 ℃; for 48h; Inert atmosphere;
DOI:10.1016/j.molcatb.2012.06.004
Guidance literature:
With MoO2Cl2(DMSO)2; dimethyl sulfoxide; for 0.166667h; Microwave irradiation;
DOI:10.1002/cssc.201800598
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