Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe

Base Information

Chemical Name:Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe
CAS No.:122350-64-5
Molecular Formula:C₆₉H₈₅N₇O₁₉S
Molecular Weight:1348.54
Hs Code.:

Fmoc<N<sup>1</sup>-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe

Synonyms:

Suppliers and Price of Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe

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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 Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe

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Technology Process of Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe

There total 2 articles about Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe 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:

: 122350-67-8
Phe-Phe-Pro-Leu-Met-OMe

: 122350-55-4
N-9-fluorenylmethyloxycarbonyl-1 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> glutamic acid benzyl ester

: 122350-64-5
Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe

Guidance literature:: With 4-methyl-morpholine; isobutyl chloroformate; Yield given. Multistep reaction; 2.) DMF, -15 deg C, 1 h then R_.T_., 2 h;
DOI:10.1016/S0040-4020(01)89802-1

Reference yield:

: 122350-57-6
N-9-fluorenylmethyloxycarbonyl-1 2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> glutamyl, phenylalanyl, phenylalanyl, proline methyl ester

: 72217-96-0
H-Leu-Met-OCH₃

: 122350-64-5
Fmoc1-2,3,4,6-tetra-O-acetyl-β-glcp>Glu-Phe-Phe-Pro-Leu-Met-OMe

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; Yield given. Multistep reaction; 2.) THF, -15 deg C, 1 h then R_.T_., overnight;
DOI:10.1016/S0040-4020(01)89802-1