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5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene

Base Information
  • Chemical Name:5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene
  • CAS No.:58002-98-5
  • Molecular Formula:C18H18
  • Molecular Weight:234.341
  • Hs Code.:
  • Mol file:58002-98-5.mol
5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene

Synonyms:[2.2.2](1,2,4)Cyclophane

Suppliers and Price of 5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 3 raw suppliers
Chemical Property of 5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene
Chemical Property:
  • Vapor Pressure:0.000122mmHg at 25°C 
  • Melting Point:166-168 °C 
  • Boiling Point:345.6°C at 760 mmHg 
  • Flash Point:173.3°C 
  • PSA:0.00000 
  • Density:1.1g/cm3 
  • LogP:3.66900 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene

There total 15 articles about 5,6,11,12-Tetrahydro-2,9-ethanodibenzo[a,e]cyclooctene 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 zinc; In dimethyl sulfoxide; at 55 ℃; for 4h; sealed tube, vacuum;
Guidance literature:
Multi-step reaction with 2 steps
1: 92 percent / PBr3 / CH2Cl2 / 0.5 h
2: 73 percent / Zn-powder / dimethylsulfoxide / 4 h / 55 °C / sealed tube, vacuum
With phosphorus tribromide; zinc; In dichloromethane; dimethyl sulfoxide;
Guidance literature:
Multi-step reaction with 7 steps
1: 74 percent / Aluminum chloride / CH2Cl2 / 0.25 h / -50 - -20 °C
2: 55 percent / Hydrochloric acid / 3.75 h / 55 °C
3: KOH, Bromine / dioxane / 17 h / Ambient temperature
4: 72 percent / Lithium aluminum hydride / tetrahydrofuran / 96 h / Heating
5: Acetic anhydride, p-toluenesulfonic acid / acetic acid / Heating
6: Boron trifluoride-etherate / benzene / 0.5 h / Ambient temperature
7: 1.) tosylhydrazine, sulfuric acid; 2.) sodium methoxide / 1.) Benzene, reflux, 15 min; 2.) THF, irradiation, 20 deg C, 70 min.
With hydrogenchloride; potassium hydroxide; lithium aluminium tetrahydride; aluminium trichloride; sulfuric acid; boron trifluoride diethyl etherate; bromine; sodium methylate; acetic anhydride; toluene-4-sulfonic acid; toluene-4-sulfonic acid hydrazide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; acetic acid; benzene;
DOI:10.1021/jo01308a005
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