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Chavibetol

Base Information Edit
  • Chemical Name:Chavibetol
  • CAS No.:501-19-9
  • Molecular Formula:C10H12O2
  • Molecular Weight:164.204
  • Hs Code.:2909500000
  • UNII:OE7NQ16G4D
  • DSSTox Substance ID:DTXSID70198206
  • Nikkaji Number:J6.118B
  • Wikipedia:Chavibetol
  • Wikidata:Q2961728
  • Metabolomics Workbench ID:129880
  • ChEMBL ID:CHEMBL259093
  • Mol file:501-19-9.mol
Chavibetol

Synonyms:5-allyl-2-methoxyphenol;chavibetol

Suppliers and Price of Chavibetol
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-METHOXY-5-(PROP-2-EN-1-YL)PHENOL 95.00%
  • 5MG
  • $ 495.04
Total 25 raw suppliers
Chemical Property of Chavibetol Edit
Chemical Property:
  • Vapor Pressure:0.0114mmHg at 25°C 
  • Melting Point:8.5°C 
  • Refractive Index:1.535 
  • Boiling Point:253.5 °C at 760 mmHg 
  • PKA:10.00±0.10(Predicted) 
  • Flash Point:122.4 °C 
  • PSA:29.46000 
  • Density:1.05 g/cm3 
  • LogP:2.12930 
  • XLogP3:2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:164.083729621
  • Heavy Atom Count:12
  • Complexity:145
Purity/Quality:

99%, *data from raw suppliers

2-METHOXY-5-(PROP-2-EN-1-YL)PHENOL 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=C(C=C(C=C1)CC=C)O
Technology Process of Chavibetol

There total 17 articles about Chavibetol 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 lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; for 3.5h;
DOI:10.1248/cpb.c18-00197

Reference yield: 72.0%

Guidance literature:
Estragole; With N,N,N,N,-tetramethylethylenediamine; sec.-butyllithium; In tetrahydrofuran; cyclohexane; at -78 ℃; for 2h;
With Trimethyl borate; In tetrahydrofuran; cyclohexane; at 0 ℃; for 1h;
With dihydrogen peroxide; sodium hydroxide; In tetrahydrofuran; cyclohexane; water; at 20 ℃; for 2h;
DOI:10.1002/anie.201608526
Guidance literature:
With caesium carbonate; In 2,2,2-trifluoroethanol; for 18h; Irradiation;
DOI:10.1039/b506735a
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