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alpha-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol

Base Information Edit
  • Chemical Name:alpha-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol
  • CAS No.:101910-24-1
  • Molecular Formula:C22H25NO2
  • Molecular Weight:335.446
  • Hs Code.:
  • European Community (EC) Number:634-425-3
  • UNII:WNW5RYD8MG
  • DSSTox Substance ID:DTXSID00906795
  • Nikkaji Number:J291.659B
  • Wikidata:Q27163617
  • Pharos Ligand ID:UBXH4TPP18G7
  • ChEMBL ID:CHEMBL8747
  • Mol file:101910-24-1.mol
alpha-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol

Synonyms:alpha-pentyl-3-(2-quinolinylmethoxy)benzenemethanol;PF 5901;PF-5901;REV 5901;REV-5901;RG 5901;RG-5901

Suppliers and Price of alpha-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol
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
  • L-655,238
  • 25mg
  • $ 145.00
  • Cayman Chemical
  • REV 5901 ≥98%
  • 50mg
  • $ 200.00
  • Cayman Chemical
  • REV 5901 ≥98%
  • 100mg
  • $ 350.00
  • Cayman Chemical
  • REV 5901 ≥98%
  • 10mg
  • $ 48.00
  • Cayman Chemical
  • REV 5901 ≥98%
  • 5mg
  • $ 25.00
  • ApexBio Technology
  • REV5901
  • 10mg
  • $ 67.00
  • ApexBio Technology
  • REV5901
  • 50mg
  • $ 277.00
  • ApexBio Technology
  • REV5901
  • 100mg
  • $ 485.00
  • American Custom Chemicals Corporation
  • REV 5901 95.00%
  • 5MG
  • $ 431.50
  • American Custom Chemicals Corporation
  • REV 5901 95.00%
  • 100MG
  • $ 926.00
Total 7 raw suppliers
Chemical Property of alpha-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol Edit
Chemical Property:
  • Vapor Pressure:1E-10mmHg at 25°C 
  • Refractive Index:1.606 
  • Boiling Point:497.7 °C at 760 mmHg 
  • PKA:14.48±0.20(Predicted) 
  • Flash Point:254.8 °C 
  • PSA:42.35000 
  • Density:1.123 g/cm3 
  • LogP:5.42750 
  • Solubility.:≤100mg/ml in ethanol;100mg/ml in methanol;100mg/ml in acetone;100mg/ml in DMSO;100mg/ml in etonitrile. 
  • XLogP3:5.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:8
  • Exact Mass:335.188529040
  • Heavy Atom Count:25
  • Complexity:375
Purity/Quality:

98%min *data from raw suppliers

L-655,238 *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCCCCC(C1=CC(=CC=C1)OCC2=NC3=CC=CC=C3C=C2)O
  • Description REV 5901 is an antagonist of cysteinyl-leukotriene receptors with a Ki value of 0.7 μM for guinea pig lung membranes. It is also an inhibitor of rat neutrophil 5-LO with an IC50 value of 0.12 μM.
  • Uses REV 5901 is an antagonist of cysteinyl-leukotriene receptors with a Ki value of 0.7 μM for guinea pig lung membranes. It is also an inhibitor of rat neutrophil 5-LO with an IC50 value of 0.12 μM. L-655,238 is a potent and selective inhibitor of FLAP (5-LO-activating protein).
Technology Process of alpha-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol

There total 9 articles about alpha-Pentyl-3-(2-quinolinylmethoxy)benzenemethanol 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 potassium carbonate; In N,N-dimethyl-formamide; at 75 ℃; for 20h;
DOI:10.1021/jo00064a043
Guidance literature:
Multi-step reaction with 4 steps
1: 1) lithium diisopropylamide / 1) THF, -78 deg C, 1 h, 2) THF, -78 deg C, 0.3 h
2: 80 percent / p-toluenesulfonic acid monohydrate, 3 Angstroem molecular sieves / toluene / 22 h / 40 °C
3: 98 percent / H2 / 10percent Pd-C / ethanol / 1 h / 25 °C / 760 Torr
4: 86 percent / K2CO3 / dimethylformamide / 20 h / 75 °C
With 3 A molecular sieve; hydrogen; potassium carbonate; toluene-4-sulfonic acid; lithium diisopropyl amide; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo00064a043
Guidance literature:
Multi-step reaction with 2 steps
1: 98 percent / H2 / 10percent Pd-C / ethanol / 1 h / 25 °C / 760 Torr
2: 86 percent / K2CO3 / dimethylformamide / 20 h / 75 °C
With hydrogen; potassium carbonate; palladium on activated charcoal; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jo00064a043
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