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Grevillol

Base Information Edit
  • Chemical Name:Grevillol
  • CAS No.:5259-01-8
  • Molecular Formula:C19H32 O2
  • Molecular Weight:292.462
  • Hs Code.:2907299090
  • European Community (EC) Number:664-084-6
  • DSSTox Substance ID:DTXSID60200564
  • Nikkaji Number:J13.505D
  • Wikidata:Q27106804
  • Metabolomics Workbench ID:68324
  • ChEMBL ID:CHEMBL451044
  • Mol file:5259-01-8.mol
Grevillol

Synonyms:5-tridecyl-1,2-benzenediol;grevillol

Suppliers and Price of Grevillol
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
  • TRC
  • 5-Tridecylresorcinol
  • 500mg
  • $ 1295.00
  • TRC
  • 5-Tridecylresorcinol
  • 100mg
  • $ 305.00
  • TRC
  • 5-Tridecylresorcinol
  • 10mg
  • $ 90.00
Total 0 raw suppliers
Chemical Property of Grevillol Edit
Chemical Property:
  • Vapor Pressure:7.26E-08mmHg at 25°C 
  • Boiling Point:426.2°C at 760 mmHg 
  • Flash Point:187.6°C 
  • PSA:40.46000 
  • Density:0.972g/cm3 
  • LogP:5.95130 
  • Storage Temp.:2-8°C 
  • XLogP3:8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:12
  • Exact Mass:292.240230259
  • Heavy Atom Count:21
  • Complexity:220
Purity/Quality:

5-Tridecylresorcinol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 41-43 
  • Safety Statements: 26-36/37-39 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCC1=CC(=CC(=C1)O)O
  • Uses 5-Tridecylresorcinol and other resorcinol derivatives have been used to study the cytotoxic and antifungal apotential
Technology Process of Grevillol

There total 19 articles about Grevillol 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 hydrogen bromide; acetic acid; for 3h; Heating;
DOI:10.1021/jo9610624
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) Mg, I2
2: p-TsOH / benzene
3: 89 percent / H2 / 10percent Pd/C
4: BBr3 / CH2Cl2
With hydrogen; iodine; boron tribromide; toluene-4-sulfonic acid; magnesium; palladium on activated charcoal; In dichloromethane; benzene;
DOI:10.1021/ja00156a004
Guidance literature:
Multi-step reaction with 2 steps
1: H2 / 10percent Pd/C / ethyl acetate / 12 h / 25 °C
2: BBr3 / CH2Cl2 / 12 h / 0 - 25 °C
With hydrogen; boron tribromide; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1021/ja00219a046
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