<β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2

Base Information

Chemical Name:<β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2
CAS No.:138093-23-9
Molecular Formula:C₈₄H₁₀₉N₁₇O₁₆S₄
Molecular Weight:1741.16
Hs Code.:

Synonyms:<β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2

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Chemical Property of <β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2

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Technology Process of <β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2

There total 1 articles about <β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2 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: 64.6%

: 2407-76-3
Arg(Tos)-NH₂

: 110551-31-0
<(β-benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)

: 138093-23-9
<β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; for 6h; Ambient temperature;
DOI:10.1021/jm00080a027

Reference yield:

: 138093-23-9
<β-(benzylthio)-β,β-pentamethylenepropionyl>-Tyr(Me)-Phe-Gln-Asn-Cys(Bzl)-Pro-Arg(Tos)-Arg(Tos)-NH2

: 138093-13-7
C₅₆H₈₃N₁₇O₁₂S₂

Guidance literature:: With ammonia; sodium; potassium hexacyanoferrate(III); Yield given. Multistep reaction; 1.) reflux, 30 s, 2.) water, 20 min;
DOI:10.1021/jm00080a027