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trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate

Base Information Edit
  • Chemical Name:trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate
  • CAS No.:57405-08-0
  • Molecular Formula:C34H22O4
  • Molecular Weight:494.546
  • Hs Code.:
  • Mol file:57405-08-0.mol
trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate

Synonyms:

Suppliers and Price of trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate
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
  • trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyreneDibenzoate
  • 5mg
  • $ 165.00
  • Medical Isotopes, Inc.
  • trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyreneDibenzoate
  • 50 mg
  • $ 2200.00
Total 0 raw suppliers
Chemical Property of trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate Edit
Chemical Property:
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Benzene, Chloroform, Tetrahydrofuran 
Purity/Quality:

trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyreneDibenzoate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Protected trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene (D452280), a metabolite of Benzopyrene (B205800). A carcinogen.
Technology Process of trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate

There total 5 articles about trans-7,8-Dihydroxy-7,8-dihydrobenzo[a]pyrene Dibenzoate 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:
Multi-step reaction with 3 steps
1: 60 percent / I2
2: 57 percent / NBS
3: 50 percent / xylene
With N-Bromosuccinimide; iodine; In xylene;
Guidance literature:
Multi-step reaction with 4 steps
1: 3.64 g / p-TsOH / benzene / 1 h / 50 °C
2: 60 percent / I2
3: 57 percent / NBS
4: 50 percent / xylene
With N-Bromosuccinimide; iodine; toluene-4-sulfonic acid; In xylene; benzene;
Refernces Edit
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