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IMinostilbene-10,11-dihydrodiol

Base Information
  • Chemical Name:IMinostilbene-10,11-dihydrodiol
  • CAS No.:56211-73-5
  • Molecular Formula:C14H13NO2
  • Molecular Weight:227.263
  • Hs Code.:
  • Mol file:56211-73-5.mol
IMinostilbene-10,11-dihydrodiol

Synonyms:10,11-dihydro-5H-dibenzo[b,f]azepine-10,11-diol

Suppliers and Price of IMinostilbene-10,11-dihydrodiol
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
  • Iminostilbene-10,11-dihydrodiol
  • 100mg
  • $ 460.00
  • TRC
  • Iminostilbene-10,11-dihydrodiol
  • 1g
  • $ 1190.00
  • Medical Isotopes, Inc.
  • Iminostilbene-10,11-dihydrodiol
  • 1 g
  • $ 2200.00
  • Medical Isotopes, Inc.
  • Iminostilbene-10,11-dihydrodiol
  • 100 mg
  • $ 650.00
Total 5 raw suppliers
Chemical Property of IMinostilbene-10,11-dihydrodiol
Chemical Property:
  • Melting Point:>128°C (dec.) 
  • Storage Temp.:Refrigerator 
  • Solubility.:Acetone, DMSO, Methanol 
Purity/Quality:

≥95% *data from raw suppliers

Iminostilbene-10,11-dihydrodiol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Iminostilbene-10,11-dihydrodiol is a metabolite of Carbamazepine 10,11-Epoxide (C175850).
Technology Process of IMinostilbene-10,11-dihydrodiol

There total 1 articles about IMinostilbene-10,11-dihydrodiol 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 1,4-diaza-bicyclo[2.2.2]octane; potassium osmate(VI); 4-methylmorpholine N-oxide; In acetone; at 20 ℃; for 24h;
DOI:10.1039/b506409k
Guidance literature:
Multi-step reaction with 4 steps
1: 85 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / dioxane / 10 h / 15 °C
2: 55 percent / aq. NH4NO3; Cu(OAc)2 / acetic acid / 0.5 h / 80 °C
3: 85 percent / p-toluenesulfonic acid / CHCl3 / 10 h / Heating
4: 82 percent / t-BuONa; P(t-Bu)3 / Pd2(dba)3 / toluene / 8 h / Heating
With ammonium nitrate; copper diacetate; tri-tert-butyl phosphine; toluene-4-sulfonic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium t-butanolate; tris(dibenzylideneacetone)dipalladium (0); In 1,4-dioxane; chloroform; acetic acid; toluene;
DOI:10.1039/b506409k
Guidance literature:
Multi-step reaction with 4 steps
1: 85 percent / 2,3-dichloro-5,6-dicyano-1,4-benzoquinone / dioxane / 10 h / 15 °C
2: 55 percent / aq. NH4NO3; Cu(OAc)2 / acetic acid / 0.5 h / 80 °C
3: 85 percent / p-toluenesulfonic acid / CHCl3 / 10 h / Heating
4: 87 percent / t-BuONa; P(t-Bu)3 / Pd2(dba)3 / toluene / 8 h / Heating
With ammonium nitrate; copper diacetate; tri-tert-butyl phosphine; toluene-4-sulfonic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; sodium t-butanolate; tris(dibenzylideneacetone)dipalladium (0); In 1,4-dioxane; chloroform; acetic acid; toluene;
DOI:10.1039/b506409k
upstream raw materials:

dibenzoazepine

Downstream raw materials:

5H-dibenzazepine-10(11H),11-dione

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