C₃₉H₅₈N₂O₁₁

Base Information

Chemical Name:C₃₉H₅₈N₂O₁₁
CAS No.:850146-60-0
Molecular Formula:C₃₉H₅₈N₂O₁₁
Molecular Weight:730.896
Hs Code.:

C<sub>39</sub>H<sub>58</sub>N<sub>2</sub>O<sub>11</sub>

Synonyms:C₃₉H₅₈N₂O₁₁

Suppliers and Price of C₃₉H₅₈N₂O₁₁

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

Total 0 raw suppliers

Chemical Property of C₃₉H₅₈N₂O₁₁

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₉H₅₈N₂O₁₁

There total 1 articles about C₃₉H₅₈N₂O₁₁ 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:

Reference yield:

: 42564-51-2
4-fluoro-3-nitrobenzaldehyde

: 850146-60-0
C₃₉H₅₈N₂O₁₁

Guidance literature:: Multi-step reaction with 6 steps

1.1: pyridinium p-toluenesulfonate / CH₂Cl₂

2.1: 60 percent / potassium bis(trimethylsilyl)amide / tetrahydrofuran / 0 °C

3.1: sodium borohydride; methanol / NiCl₂*xH₂O / 10 h / 0 °C

4.1: potassium carbonate / methanol / 72 h

5.1: triethylamine / CH₂Cl₂

5.2: aq. HCl / ethanol / 0.5 h / Heating

6.1: 63 percent / EDCI; pyridinium trifluoroacetate; DMSO / CH₂Cl₂

With methanol; sodium tetrahydroborate; pyridinium trifluroacetate; pyridinium p-toluenesulfonate; potassium hexamethylsilazane; potassium carbonate; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; nickel dichloride; In tetrahydrofuran; methanol; dichloromethane; 4.1: Michael addition / 6.1: Pfitzner-Moffat reaction;
DOI:10.1016/j.tetlet.2005.01.126