α-BOC-di-ε-Z-lysyllysine

Base Information

Chemical Name:α-BOC-di-ε-Z-lysyllysine
CAS No.:27317-71-1
Molecular Formula:C₃₃H₄₆N₄O₉
Molecular Weight:642.75
Hs Code.:

Synonyms:α-BOC-di-ε-Z-lysyllysine

Suppliers and Price of α-BOC-di-ε-Z-lysyllysine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 1 raw suppliers

Chemical Property of α-BOC-di-ε-Z-lysyllysine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of α-BOC-di-ε-Z-lysyllysine

There total 9 articles about α-BOC-di-ε-Z-lysyllysine 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: 88.0%

: 27317-68-6
Boc-Lys(Z)-Lys(Z)-OMe

: 27317-71-1
α-BOC-di-ε-Z-lysyllysine

Guidance literature:: With sodium hydroxide; In methanol; at 20 ℃; for 2h;
DOI:10.1021/jo061144k

Reference yield: 71.0%

: N-ε-Cbz-L-lysine TFA salt

: 2389-45-9
Boc-Lys(Z)-OH

: 27317-71-1
α-BOC-di-ε-Z-lysyllysine

Guidance literature:: With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 24.5h;
DOI:10.1002/chem.200306062

Reference yield:

: 2389-45-9
Boc-Lys(Z)-OH

: 27317-71-1
α-BOC-di-ε-Z-lysyllysine

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / EDCI*HCl; HOBt; N-methylmorpholine / CH₂Cl₂ / 0 - 20 °C

2: 88 percent / aq. NaOH / methanol / 2 h / 20 °C

With 4-methyl-morpholine; sodium hydroxide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane;
DOI:10.1021/jo061144k