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2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy-

Base Information
  • Chemical Name:2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy-
  • CAS No.:68112-21-0
  • Molecular Formula:C24H40O4
  • Molecular Weight:392.57
  • Hs Code.:
2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy-

Synonyms:Elasnin;

Suppliers and Price of 2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy-
Supply Marketing:
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
  • Usbiological
  • Elasnin
  • 1mg
  • $ 358.00
  • TRC
  • Elasnin
  • 5mg
  • $ 390.00
  • Cayman Chemical
  • Elasnin ≥98%
  • 5mg
  • $ 417.00
  • American Custom Chemicals Corporation
  • 3,5-DIBUTYL-6-(1-BUTYL-2-OXOHEPTYL)-4-HYDROXY-2H-PYRAN-2-ONE 95.00%
  • 5MG
  • $ 504.78
  • Adipogen Life Sciences
  • Elasnin ≥97%(HPLC)
  • 1 mg
  • $ 130.00
Total 5 raw suppliers
Chemical Property of 2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy-
Chemical Property:
  • Vapor Pressure:4.96E-13mmHg at 25°C 
  • Boiling Point:521°C at 760 mmHg 
  • Flash Point:166.6°C 
  • PSA:67.51000 
  • Density:1.001g/cm3 
  • LogP:6.45380 
Purity/Quality:

98% *data from raw suppliers

Elasnin *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Elasnin is a natural compound isolated from Streptomyces. It is a reversible inhibitor of human granulocyte elastase.
Technology Process of 2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy-

There total 9 articles about 2H-Pyran-2-one, 3,5-dibutyl-6-(1-butyl-2-oxoheptyl)-4-hydroxy- 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 sulfuric acid; at 0 ℃; for 0.0833333h;
DOI:10.1016/S0040-4039(00)74555-2
Guidance literature:
With pyridine; chromium(VI) oxide; In acetone; at 0 - 20 ℃;
DOI:10.1021/jo00352a035
Guidance literature:
Multi-step reaction with 4 steps
1: 88 percent / m-chloroperoxybenzoic acid, 4,4'-thiobis-(6-t-butyl-3-methylphenol) / 1,2-dichloro-ethane / 9 h / Ambient temperature
2: H2 / 10percent Pd-C / ethanol / Ambient temperature
3: oxidation with Jones reagent
4: 92 percent / conc. H2SO4 / 0.08 h / 0 °C
With Santonox R; sulfuric acid; hydrogen; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In ethanol; 1,2-dichloro-ethane;
DOI:10.1016/S0040-4039(00)74555-2
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