tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

Base Information

Chemical Name:tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate
CAS No.:1356009-16-9
Molecular Formula:C₁₇H₂₁ClN₄O₅
Molecular Weight:396.831
Hs Code.:
Mol file:1356009-16-9.mol

Synonyms:tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

Suppliers and Price of tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

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 tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

There total 6 articles about tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate 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: 66.6%

: 1356009-15-8
tert-butyl 3-(2-chloro-5-nitrophenoxy)propylcarbamate

: 15965-31-8
4-chloro-1H-imidazole

: 1356009-16-9
tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

Guidance literature:: With potassium hydroxide; In dimethyl sulfoxide; at 90 ℃; for 18h;

Reference yield:

: 58885-58-8
N-tert-butoxycarbonyl-3-aminopropanol

: 1356009-16-9
tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: carbon tetrabromide; triphenylphosphine / dichloromethane / 18 h / 0 - 20 °C

2: caesium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 18 h / 20 °C

3: potassium hydroxide / dimethyl sulfoxide / 18 h / 90 °C

With carbon tetrabromide; caesium carbonate; triphenylphosphine; potassium hydroxide; tetra-(n-butyl)ammonium iodide; In dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 83948-53-2
3-bromopropylamine tert-butylcarbamate

: 1356009-16-9
tert-butyl 3-(2-(4-chloro-1H-imidazol-1-yl)-5-nitrophenoxy)propylcarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: caesium carbonate / tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 18 h / 20 °C

2: potassium hydroxide / dimethyl sulfoxide / 18 h / 90 °C

With caesium carbonate; potassium hydroxide; tetra-(n-butyl)ammonium iodide; In dimethyl sulfoxide; N,N-dimethyl-formamide;