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Encyclopedia

Phe-Thr

Base Information Edit
  • Chemical Name:Phe-Thr
  • CAS No.:51352-44-4
  • Molecular Formula:C13H18N2O4
  • Molecular Weight:266.297
  • Hs Code.:
  • Wikidata:Q27142890
  • Mol file:51352-44-4.mol
Phe-Thr

Synonyms:Phe-Thr;L-phenylalanyl-L-threonine;Phenylalanyl-Threonine;phenylalanylthreonine;FT dipeptide;F-T Dipeptide;L-Phe-L-Thr;SCHEMBL8525812;Phenylalanine Threonine dipeptide;Phenylalanine-Threonine dipeptide;CHEBI:73636;Q27142890;F-T

Suppliers and Price of Phe-Thr
Supply Marketing:Edit
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-Thr Edit
Chemical Property:
  • XLogP3:-3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:266.12665706
  • Heavy Atom Count:19
  • Complexity:316
Purity/Quality:

≥98% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(C(C(=O)O)NC(=O)C(CC1=CC=CC=C1)N)O
  • Isomeric SMILES:C[C@H]([C@@H](C(=O)O)NC(=O)[C@H](CC1=CC=CC=C1)N)O
Technology Process of Phe-Thr

There total 7 articles about Phe-Thr 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:
Guidance literature:
With hydrogen; palladium; In methanol;
Guidance literature:
Fmoc-Thr(tBu)-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
Guidance literature:
Multi-step reaction with 3 steps
1: 66 percent / dimethylformamide
2: 67 percent / NaOH / dioxane; H2O
3: 82 percent / H2 / Pd / methanol
With sodium hydroxide; hydrogen; palladium; In 1,4-dioxane; methanol; water; N,N-dimethyl-formamide;
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