(N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester

Base Information

Chemical Name:(N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester
CAS No.:1053209-10-1
Molecular Formula:C₃₀H₃₅N₃O₇
Molecular Weight:549.624
Hs Code.:

Synonyms:(N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester

Suppliers and Price of (N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester

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 (N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester

There total 1 articles about (N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester 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: 91.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 55782-87-1
N-carbobenzyloxy-L-tryptophanyl-L-proline methyl ester

: 1053209-10-1
(N-carbobenzyloxy-1-tert-butoxycarbonyl-L-tryptophanyl)-L-proline methyl ester

Guidance literature:: N-carbobenzyloxy-L-tryptophanyl-L-proline methyl ester; With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; for 0.25h; Inert atmosphere;

di-tert-butyl dicarbonate; In dichloromethane; Inert atmosphere;
DOI:10.1021/ol8015513