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L-Phenylalanine, L-leucyl-, phenylmethyl ester (monotrifluoroacetate)

Base Information
  • Chemical Name:L-Phenylalanine, L-leucyl-, phenylmethyl ester (monotrifluoroacetate)
  • CAS No.:70637-28-4
  • Molecular Formula:C2HF3O2*C22H28N2O3
  • Molecular Weight:482.5
  • Hs Code.:
  • Mol file:70637-28-4.mol
L-Phenylalanine, L-leucyl-, phenylmethyl ester (monotrifluoroacetate)

Synonyms:(S)-benzyl 2-((S)-2-amino-4-methylpentanamido)-3-phenylpropanoate TFA salt

Suppliers and Price of L-Phenylalanine, L-leucyl-, phenylmethyl ester (monotrifluoroacetate)
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
  • ChemScene
  • L-Phenylalanine,L-leucyl-,phenylmethylestermonotrifluoroacetate
  • 1g
  • $ 450.00
Total 8 raw suppliers
Chemical Property of L-Phenylalanine, L-leucyl-, phenylmethyl ester (monotrifluoroacetate)
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

L-Phenylalanine,L-leucyl-,phenylmethylestermonotrifluoroacetate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of L-Phenylalanine, L-leucyl-, phenylmethyl ester (monotrifluoroacetate)

There total 3 articles about L-Phenylalanine, L-leucyl-, phenylmethyl ester (monotrifluoroacetate) 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:
Multi-step reaction with 2 steps
1: N-ethyl-N,N-diisopropylamine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / 16 h / 0 - 20 °C / Inert atmosphere; Green chemistry
2: 3 h / 20 °C / Inert atmosphere; Green chemistry
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine;
DOI:10.1039/c7gc00247e
Guidance literature:
Multi-step reaction with 2 steps
1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 3 h / 0 - 20 °C
2: dichloromethane / 5 h / 0 - 20 °C
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.8b01201
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