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Bilobol

Base Information Edit
  • Chemical Name:Bilobol
  • CAS No.:22910-86-7
  • Molecular Formula:C21H34 O2
  • Molecular Weight:318.5
  • Hs Code.:2907299090
  • UNII:NSK9KWM3T6
  • ChEMBL ID:CHEMBL461628
  • DSSTox Substance ID:DTXSID90872874
  • Metabolomics Workbench ID:53010
  • Nikkaji Number:J167.340H
  • Wikidata:Q4913564
  • Wikipedia:Bilobol
  • Mol file:22910-86-7.mol
Bilobol

Synonyms:5-(8-pentadecenyl)-1,3-benzenediol;bilobol

Suppliers and Price of Bilobol
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
Total 4 raw suppliers
Chemical Property of Bilobol Edit
Chemical Property:
  • Vapor Pressure:5.37E-09mmHg at 25°C 
  • Melting Point:32 °C 
  • Boiling Point:457.7°C at 760 mmHg 
  • PKA:9.55±0.10(Predicted) 
  • Flash Point:199.3°C 
  • PSA:40.46000 
  • Density:0.97g/cm3 
  • LogP:6.67840 
  • XLogP3:8.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:13
  • Exact Mass:318.255880323
  • Heavy Atom Count:23
  • Complexity:278
Purity/Quality:

99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCC=CCCCCCCCC1=CC(=CC(=C1)O)O
  • Isomeric SMILES:CCCCCC/C=C\CCCCCCCC1=CC(=CC(=C1)O)O
Technology Process of Bilobol

There total 8 articles about Bilobol 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:
Multi-step reaction with 2 steps
1: 87 percent / H2, quinoline / 5percent Pd/CaCO3 / cyclohexane / 1 h / 760 Torr
2: 92 percent / MeMgI / 0.25 h / 100 - 165 °C
With quinoline; methyl magnesium iodide; hydrogen; Lindlar's catalyst; In cyclohexane;
DOI:10.1021/ja00156a004
Guidance literature:
Multi-step reaction with 3 steps
1: 90 percent / tetrahydrofuran; hexamethylphosphoric acid triamide / 7.5 h / Heating
3: 96 percent / 9-iodo-BBN / hexane / Ambient temperature
With 9-iodo-BBN; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane;
DOI:10.1021/jo962423i
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) n-BuLi, hexamethylphosphoramide / 1.) hexane, 0 deg C, 30 min, 2.) THF, RT, 12 h
2: 87 percent / H2, quinoline / 5percent Pd/CaCO3 / cyclohexane / 1 h / 760 Torr
3: 92 percent / MeMgI / 0.25 h / 100 - 165 °C
With quinoline; N,N,N,N,N,N-hexamethylphosphoric triamide; methyl magnesium iodide; n-butyllithium; hydrogen; Lindlar's catalyst; In cyclohexane;
DOI:10.1021/ja00156a004
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