c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine

Base Information

Chemical Name:c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine
CAS No.:1187754-67-1
Molecular Formula:C₃₂H₄₄N₄O₆
Molecular Weight:580.725
Hs Code.:

Synonyms:c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine

Suppliers and Price of c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine

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

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Chemical Property of c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine

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Technology Process of c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine

There total 1 articles about c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine 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:

: 918663-78-2
2-(9H-fluoren-9-ylmethoxycarbonylamino)-octanedioic acid 1-allyl ester 8-tert-butyl ester

: 35661-60-0
Fmoc-Leu-OH

: 96402-49-2,138774-93-3
N^α-Fmoc-3-(1'-naphthyl)alanine

: 94744-50-0
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid

: 1187754-67-1
c[Asu-Nal-β3Leu-Aib]; Asu = (S)-2-aminosuberic acid; Nal = 1-naphthylalanine

Guidance literature:: 2-(9H-fluoren-9-ylmethoxycarbonylamino)-octanedioic acid 1-allyl ester 8-tert-butyl ester; With trifluoroacetic acid; In dichloromethane; for 1h;

N^α-Fmoc-3-(1'-naphthyl)alanine; With benzotriazol-1-ol; diisopropyl-carbodiimide; solid phase reaction;

Fmoc-Leu-OH; N-[(9H-fluoren-9-ylmethoxy)carbonyl]-α-aminoisobutyric acid; Further stages;
DOI:10.1021/jm900850t