Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

Base Information

Chemical Name:Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl
CAS No.:99909-25-8
Molecular Formula:C₄₃H₆₀N₆O₉
Molecular Weight:804.984
Hs Code.:

Synonyms:Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

Suppliers and Price of Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

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 Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

There total 8 articles about Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl 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: 95.0%

: 60079-62-1
H-Leu-Gly-OBzl*HCl

: 99909-24-7
Z-Pro-Val-Leu-Gly-OH

: 99909-25-8
Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

Guidance literature:: With 4-methyl-morpholine; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 0 ℃; for 3h;

Reference yield:

: 13139-15-6,53296-34-7
N-tert-butoxycarbonyl-L-leucine

: 99909-25-8
Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / NMM, ECF / tetrahydrofuran; dimethylformamide / 1 h on ice bath, then room temperature

2: 98 percent / 3.5 N HCl / dioxane / 1 h / Ambient temperature

3: 95 percent / NMM, DCC, HOBt / dimethylformamide / 3 h / 0 °C

With 4-methyl-morpholine; hydrogenchloride; chloroformic acid ethyl ester; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 37783-45-2
Boc-L-Leu-Gly-OBzl

: 99909-25-8
Z-Pro-Val-Leu-Gly-Pro-Val-O-Bzl

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / 3.5 N HCl / dioxane / 1 h / Ambient temperature

2: 95 percent / NMM, DCC, HOBt / dimethylformamide / 3 h / 0 °C

With 4-methyl-morpholine; hydrogenchloride; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In 1,4-dioxane; N,N-dimethyl-formamide;