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N-succinimidyl (2S)-2-{N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino}propionate

Base Information Edit
  • Chemical Name:N-succinimidyl (2S)-2-{N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino}propionate
  • CAS No.:89371-34-6
  • Molecular Formula:C19H24N2O6
  • Molecular Weight:376.409
  • Hs Code.:
  • Mol file:89371-34-6.mol
N-succinimidyl (2S)-2-{N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino}propionate

Synonyms:N-succinimidyl (2S)-2-{N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino}propionate

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-succinimidyl (2S)-2-{N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino}propionate Edit
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Technology Process of N-succinimidyl (2S)-2-{N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino}propionate

There total 17 articles about N-succinimidyl (2S)-2-{N-[(1S)-1-(ethoxycarbonyl)-3-phenylpropyl]amino}propionate 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 8 steps
1: 28percent aq. NH3 / 168 h / Ambient temperature
3: CoCl2 / H2O / 72 h / 37 °C / aminoacylase (from Aspergillus oryzae); pH 7
4: SOCl2
5: 43.6 percent / K2CO3 / dimethylsulfoxide / 30 h / Ambient temperature
6: ethyl acetate; diisopropyl ether
7: 96 percent / H2 / Pd / ethanol / 3 h / 760 Torr / Ambient temperature
8: DCC / tetrahydrofuran / Ambient temperature
With ammonium hydroxide; thionyl chloride; hydrogen; potassium carbonate; dicyclohexyl-carbodiimide; palladium; In tetrahydrofuran; ethanol; di-isopropyl ether; water; dimethyl sulfoxide; ethyl acetate;
DOI:10.1021/jm00122a003
Guidance literature:
Multi-step reaction with 8 steps
1: 28percent aq. NH3 / 168 h / Ambient temperature
3: CoCl2 / H2O / 72 h / 37 °C / aminoacylase (from Aspergillus oryzae); pH 7
4: SOCl2
5: 27.8 percent / K2CO3 / dimethylsulfoxide / 30 h / Ambient temperature
6: ethanolic HCl
7: 95.1 percent / H2 / Pd / ethanol / 3 h / 760 Torr / Ambient temperature
8: DCC / tetrahydrofuran / Ambient temperature
With hydrogenchloride; ammonium hydroxide; thionyl chloride; hydrogen; potassium carbonate; dicyclohexyl-carbodiimide; palladium; In tetrahydrofuran; ethanol; water; dimethyl sulfoxide;
DOI:10.1021/jm00122a003
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