Boc-Asp(OBzl)-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc

Base Information

Chemical Name:Boc-Asp(OBzl)-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc
CAS No.:125421-21-8
Molecular Formula:C₉₅H₁₂₅Cl₃N₁₄O₂₃
Molecular Weight:1937.48
Hs Code.:

Synonyms:Boc-Asp(OBzl)-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc

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Chemical Property of Boc-Asp(OBzl)-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc

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Technology Process of Boc-Asp(OBzl)-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc

There total 1 articles about Boc-Asp(OBzl)-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc 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:

: 13798-75-9
N^α-t-butoxycarbonylaspartic acid α-N-hydroxysuccinimide ester β-benzyl ester

: 109419-67-2
Boc-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc

: 125421-21-8
Boc-Asp(OBzl)-Lys(Z)-Ala-Lys(Z)-Leu-Lys(Z)-Lys(Z)-Thr(Bzl)-NHNH-Troc

Guidance literature:: With 4-methyl-morpholine; TFA-anisole; Yield given. Multistep reaction; 1.) 0 deg C, 40 min, 2.) DMF, r.t., 7 h;
DOI:10.1248/cpb.37.2467