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1-Isovaleryl-3,4-dihydroxybenzene

Base Information Edit
  • Chemical Name:1-Isovaleryl-3,4-dihydroxybenzene
  • CAS No.:67239-25-2
  • Molecular Formula:C11H14O3
  • Molecular Weight:194.23
  • Hs Code.:
  • Mol file:67239-25-2.mol
1-Isovaleryl-3,4-dihydroxybenzene

Synonyms:1-Butanone, 1- (3, 4-dihydroxyphenyl)-3-methyl-;3,4-Dihydroxyisovalerophenone;1-(3,4-dihydroxyphenyl)-3-methyl-butan-1-one;3-08-00-02218 (Beilstein Handbook Reference);

Suppliers and Price of 1-Isovaleryl-3,4-dihydroxybenzene
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
  • 1-(3,4-DIHYDROXYPHENYL)-3-METHYL-1-BUTANONE 95.00%
  • 5MG
  • $ 496.41
Total 6 raw suppliers
Chemical Property of 1-Isovaleryl-3,4-dihydroxybenzene Edit
Chemical Property:
  • Vapor Pressure:2.39E-06mmHg at 25°C 
  • Refractive Index:1.555 
  • Boiling Point:381 °C at 760 mmHg 
  • Flash Point:198.4 °C 
  • PSA:57.53000 
  • Density:1.158 /cm3 
  • LogP:2.32660 
Purity/Quality:

99% *data from raw suppliers

1-(3,4-DIHYDROXYPHENYL)-3-METHYL-1-BUTANONE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of 1-Isovaleryl-3,4-dihydroxybenzene

There total 3 articles about 1-Isovaleryl-3,4-dihydroxybenzene 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 carbon disulfide; aluminium trichloride; und Erhitzen des vom Schwefelkohlenstoff befreiten Reaktionsgemisches auf 140grad;
DOI:10.1021/ja01268a003
Guidance literature:
With carbon disulfide; aluminium trichloride; und Erhitzen des vom Schwefelkohlenstoff befreiten Reaktionsgemisches auf 140grad;
DOI:10.1021/ja01268a003

Reference yield:

Guidance literature:
With aluminium trichloride; nitrobenzene; anfangs unter Kuehlung,zuletzt bei 80grad;
upstream raw materials:

benzene-1,2-diol

isopentanoyl chloride

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