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(S)-methyl 2-(2-aminoacetamido)-3-phenylpropanoate trifluoroacetate salt

Base Information Edit
  • Chemical Name:(S)-methyl 2-(2-aminoacetamido)-3-phenylpropanoate trifluoroacetate salt
  • CAS No.:203053-87-6
  • Molecular Formula:C2HF3O2*C12H16N2O3
  • Molecular Weight:350.295
  • Hs Code.:
  • Mol file:203053-87-6.mol
(S)-methyl 2-(2-aminoacetamido)-3-phenylpropanoate trifluoroacetate salt

Synonyms:(S)-methyl 2-(2-aminoacetamido)-3-phenylpropanoate trifluoroacetate salt

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Chemical Property of (S)-methyl 2-(2-aminoacetamido)-3-phenylpropanoate trifluoroacetate salt Edit
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Technology Process of (S)-methyl 2-(2-aminoacetamido)-3-phenylpropanoate trifluoroacetate salt

There total 4 articles about (S)-methyl 2-(2-aminoacetamido)-3-phenylpropanoate trifluoroacetate salt 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: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 0 - 20 °C
2: dichloromethane
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/chem.201501850
Guidance literature:
Multi-step reaction with 3 steps
1: thionyl chloride / 0 - 20 °C
2: O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine / N,N-dimethyl-formamide / 0 - 20 °C
3: dichloromethane
With thionyl chloride; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/chem.201501850
Guidance literature:
Multi-step reaction with 2 steps
1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 0 - 20 °C
2: dichloromethane / 3 h / 0 - 20 °C
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1016/j.bmc.2019.07.044
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