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3,8-Dimethylacenaphthenequinone

Base Information
  • Chemical Name:3,8-Dimethylacenaphthenequinone
  • CAS No.:146885-81-6
  • Molecular Formula:C14H10O2
  • Molecular Weight:210.232
  • Hs Code.:
  • Mol file:146885-81-6.mol
3,8-Dimethylacenaphthenequinone

Synonyms:acenaphthenequinone;3,8-dimethylacenaphthequinone;3,8-Dimethyl-acenaphthen-1,2-dion;3,8-dimethyl-acenaphthene-1,2-dione;3,8-dimethylacenaphthenequinone;2,7-Dimethylacenaphthenequinone;3,8-Dimethyl-acenaphthylene-1,2-dione;

Suppliers and Price of 3,8-Dimethylacenaphthenequinone
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
  • TRC
  • 3,8-Dimethylacenaphthenequinone
  • 100mg
  • $ 165.00
  • TCI Chemical
  • 3,8-Dimethylacenaphthenequinone >97.0%(GC)
  • 200mg
  • $ 128.00
  • TCI Chemical
  • 3,8-Dimethylacenaphthenequinone >97.0%(GC)
  • 1g
  • $ 382.00
  • AK Scientific
  • 3,8-Dimethylacenaphthenequinone
  • 200mg
  • $ 229.00
Total 7 raw suppliers
Chemical Property of 3,8-Dimethylacenaphthenequinone
Chemical Property:
  • Melting Point:204 - 205 °C 
  • Boiling Point:408.2±35.0 °C(Predicted) 
  • PSA:34.14000 
  • Density:1.310±0.06 g/cm3(Predicted) 
  • LogP:2.83560 
Purity/Quality:

98%,99%, *data from raw suppliers

3,8-Dimethylacenaphthenequinone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses 3,8-Dimethylacenaphthenequinone is a useful intermediate in the preparation of fluorinated and trifluoromethylated corannulenes.
Technology Process of 3,8-Dimethylacenaphthenequinone

There total 22 articles about 3,8-Dimethylacenaphthenequinone 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 selenium(IV) oxide; In 1,4-dioxane; water; at 60 ℃; for 48h;
DOI:10.1016/S0040-4039(00)60565-8
Guidance literature:
With aluminum tri-bromide; In dichloromethane; for 4h; cooling;
DOI:10.1021/jo071216n
Guidance literature:
Multi-step reaction with 5 steps
1: 62 percent / HCl; AcOH
2: 99 percent / acetone
3: 90 percent / H2SO4; AcOH
4: 82 percent / SOCl2; AlCl3 / CH2Cl2
5: 84 percent / SeO2 / dioxane; H2O
With hydrogenchloride; aluminium trichloride; selenium(IV) oxide; thionyl chloride; sulfuric acid; acetic acid; In 1,4-dioxane; dichloromethane; water; acetone;
DOI:10.1055/s-2003-44996
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