Phe-Gln

Base Information

Chemical Name:Phe-Gln
CAS No.:39537-24-1
Molecular Formula:C₁₄H₁₉N₃O₄
Molecular Weight:293.323
Hs Code.:
ChEMBL ID:CHEMBL2074939
Metabolomics Workbench ID:78921
Wikidata:Q27162487

Synonyms:Phe-Gln;L-phenylalanyl-L-glutamine;phenylalanylglutamine;phenylalanyl-glutamine;FQ dipeptide;F-Q Dipeptide;L-Phe-L-Gln;SCHEMBL2487636;CHEMBL2074939;Phenylalanine Glutamine dipeptide;Phenylalanine-Glutamine dipeptide;CHEBI:90354;AKOS010407211;Q27162487

Suppliers and Price of Phe-Gln

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of Phe-Gln

Chemical Property:

XLogP3:-3.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:8
Exact Mass:293.13755610
Heavy Atom Count:21
Complexity:380

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC(C(=O)NC(CCC(=O)N)C(=O)O)N
Isomeric SMILES:C1=CC=C(C=C1)C[C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)N

Technology Process of Phe-Gln

There total 2 articles about Phe-Gln 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:

: 35661-40-6
N-Fmoc L-Phe

: 132327-80-1,200623-62-7
Fmoc-L-Gln(Trt)-OH

: 39537-24-1
L-Phe-L-Gln-OH

Guidance literature:: Fmoc-L-Gln(Trt)-OH; With 1-methyl-1H-imidazole; diisopropyl-carbodiimide; at 20 ℃; for 2h; Green chemistry;

With piperidine; In N,N-dimethyl-formamide; for 0.133333h; Green chemistry;

N-Fmoc L-Phe; Further stages; Green chemistry;
DOI:10.1016/j.tetlet.2019.151058