(S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl ester

Base Information

Chemical Name:(S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl ester
CAS No.:92237-01-9
Molecular Formula:C₂₄H₃₀N₂O₅S
Molecular Weight:458.579
Hs Code.:

Synonyms:(S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl ester

Suppliers and Price of (S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl 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 (S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl ester

There total 2 articles about (S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl 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:

: 92237-00-8
Boc-Met-Glu(OBzl)2

: 92237-01-9
(S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl ester

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; ethyl acetate;

Reference yield:

: 2488-18-8
N-((tert-butyloxy)carbonyl)-L-methionine p-nitrophenyl ester

: 92237-01-9
(S)-2-((S)-2-Amino-4-methylsulfanyl-butyrylamino)-pentanedioic acid dibenzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 79 percent / hydroxybenzthiazole, N-methylmorpholine / CHCl₃ / 2 h

2: 1 N HCl / dioxane; ethyl acetate

With 4-methyl-morpholine; hydrogenchloride; 2-hydroxybenzothiazole; In 1,4-dioxane; chloroform; ethyl acetate;