Ser-phe

Base Information

Chemical Name:Ser-phe
CAS No.:16875-28-8
Molecular Formula:C12H16 N2 O4
Molecular Weight:252.27
Hs Code.:
Nikkaji Number:J151.049E
Wikidata:Q27139262
Metabolomics Workbench ID:78969
ChEMBL ID:CHEMBL3321990
Mol file:16875-28-8.mol

Synonyms:SER-PHE;H-Ser-Phe-OH;16875-28-8;Serinylphenylalanine;L-seryl-L-phenylalanine;CHEBI:71029;CHEMBL3321990;(S)-2-((S)-2-Amino-3-hydroxypropanamido)-3-phenylpropanoic acid;SF dipeptide;(2S)-2-[[(2S)-2-amino-3-hydroxypropanoyl]amino]-3-phenylpropanoic acid;(2S)-2-{[(2S)-2-amino-3-hydroxypropanoyl]amino}-3-phenylpropanoic acid;S-F Dipeptide;Seryl-phenylalanine;l-serylphenylalanine;L-Ser-L-Phe;L-Serinyl-L-Phenylalanine;N-L-Seryl-L-phenylalanine;Serine Phenylalanine dipeptide;Serine-Phenylalanine dipeptide;SCHEMBL9622556;HY-P4509;BDBM50049557;MFCD00037254;CS-0654527;Q27139262;(2S)-2-[(2S)-2-AMINO-3-HYDROXYPROPANAMIDO]-3-PHENYLPROPANOIC ACID

Suppliers and Price of Ser-phe

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

American Custom Chemicals Corporation
SER-PHE-OH 98.00%
5G
$ 1859.55

Total 11 raw suppliers

Chemical Property of Ser-phe

Chemical Property:

PSA：112.65000
LogP:0.20930
XLogP3:-3.5
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:252.11100700
Heavy Atom Count:18
Complexity:290

Purity/Quality:

99% ^*data from raw suppliers

SER-PHE-OH 98.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Ser-phe

There total 6 articles about Ser-phe 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:

: 87494-17-5
Gly-Ser-Phe

: 16875-28-8
ser-phe

: 56-40-6,18875-39-3,25718-94-9
glycine

Guidance literature:: With (Et₂NH₂)₈[{α-PW₁₁O₃₉Zr-(μ-OH)(H₂O)}₂]*7H₂O; water; 3-(trimethylsilyl)propionic-2,2,3,3-d₄acid sodium salt; In water-d2; at 60 ℃; Reagent/catalyst;
DOI:10.1002/ejic.201500161

Reference yield:

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

: 71989-33-8
Fmoc-Ser(tBu)-OH

: 16875-28-8
ser-phe

Guidance literature:: N-Fmoc L-Phe; 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;

Fmoc-Ser(tBu)-OH; Further stages; Green chemistry;
DOI:10.1016/j.tetlet.2019.151058