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benzyl (2S)-2,5-diamino-5-oxopentanoate;2,2,2-trifluoroacetic acid

Base Information
  • Chemical Name:benzyl (2S)-2,5-diamino-5-oxopentanoate;2,2,2-trifluoroacetic acid
  • CAS No.:66449-95-4
  • Molecular Formula:C12H16N2O3.C2HF3O2
  • Molecular Weight:350.295
  • Hs Code.:
benzyl (2S)-2,5-diamino-5-oxopentanoate;2,2,2-trifluoroacetic acid

Synonyms:

Suppliers and Price of benzyl (2S)-2,5-diamino-5-oxopentanoate;2,2,2-trifluoroacetic acid
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of benzyl (2S)-2,5-diamino-5-oxopentanoate;2,2,2-trifluoroacetic acid
Chemical Property:
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:7
  • Exact Mass:350.10895613
  • Heavy Atom Count:24
  • Complexity:346
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COC(=O)C(CCC(=O)N)N.C(=O)(C(F)(F)F)O
  • Isomeric SMILES:C1=CC=C(C=C1)COC(=O)[C@H](CCC(=O)N)N.C(=O)(C(F)(F)F)O
Technology Process of benzyl (2S)-2,5-diamino-5-oxopentanoate;2,2,2-trifluoroacetic acid

There total 1 articles about benzyl (2S)-2,5-diamino-5-oxopentanoate;2,2,2-trifluoroacetic acid 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 methoxybenzene; trifluoroacetic acid; at 0 ℃; for 1h;
DOI:10.1248/cpb.30.2433
Guidance literature:
With benzotriazol-1-ol; triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 24h;
DOI:10.1007/BF02758662
Guidance literature:
With triethylamine; isobutyl chloroformate; Yield given. Multistep reaction; 1.) DMF, -10 deg C, 10 min, 2.) DMF, room temp., 13 h;
DOI:10.1248/cpb.30.2433
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