ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

Base Information

Chemical Name:ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate
CAS No.:1170233-71-2
Molecular Formula:C₂₂H₃₃N₂O₄P
Molecular Weight:420.489
Hs Code.:

Synonyms:ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

Suppliers and Price of ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

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 ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

There total 6 articles about ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate 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:

: 63945-11-9
6-phthalimido-1-hexanol

: 1170233-71-2
ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

Guidance literature:: Multi-step reaction with 4 steps

1: carbon tetrabromide; triphenylphosphine / acetonitrile / 20 °C

2: 6 h / 150 °C

3: phosphorus pentachloride / toluene / Reflux

4: triethylamine / dichloromethane / 0 - 20 °C

With carbon tetrabromide; phosphorus pentachloride; triethylamine; triphenylphosphine; In dichloromethane; toluene; acetonitrile;

Reference yield:

: 908817-72-1
ethoxy(6-phthalimidohexyl)phosphinyl chloride

: 108-91-8,157973-60-9
cyclohexylamine

: 1170233-71-2
ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃;

Reference yield:

: 85-44-9
phthalic anhydride

: 1170233-71-2
ethyl N-cyclohexyl-P-(6-(1,3-dioxoisoindolin-2-yl)hexyl)phosphonamidate

Guidance literature:: Multi-step reaction with 5 steps

1: 5 h / 140 °C

2: carbon tetrabromide; triphenylphosphine / acetonitrile / 20 °C

3: 6 h / 150 °C

4: phosphorus pentachloride / toluene / Reflux

5: triethylamine / dichloromethane / 0 - 20 °C

With carbon tetrabromide; phosphorus pentachloride; triethylamine; triphenylphosphine; In dichloromethane; toluene; acetonitrile;