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ethyl (S)-3-(4-(methyl(1-(((phenylmethyl)oxy)carbonyl)-2-methylpropyl)amino)-6,7-(1,2,3,4-tetrahydro-1,1,4,4-tetramethylbenzo)-1H-indol-3-yl)-2-oximidopropionate

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  • Chemical Name:ethyl (S)-3-(4-(methyl(1-(((phenylmethyl)oxy)carbonyl)-2-methylpropyl)amino)-6,7-(1,2,3,4-tetrahydro-1,1,4,4-tetramethylbenzo)-1H-indol-3-yl)-2-oximidopropionate
  • CAS No.:134288-22-5
  • Molecular Formula:C34H45N3O5
  • Molecular Weight:575.748
  • Hs Code.:
  • Mol file:134288-22-5.mol
ethyl (S)-3-(4-(methyl(1-(((phenylmethyl)oxy)carbonyl)-2-methylpropyl)amino)-6,7-(1,2,3,4-tetrahydro-1,1,4,4-tetramethylbenzo)-1H-indol-3-yl)-2-oximidopropionate

Synonyms:ethyl (S)-3-(4-(methyl(1-(((phenylmethyl)oxy)carbonyl)-2-methylpropyl)amino)-6,7-(1,2,3,4-tetrahydro-1,1,4,4-tetramethylbenzo)-1H-indol-3-yl)-2-oximidopropionate

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Chemical Property of ethyl (S)-3-(4-(methyl(1-(((phenylmethyl)oxy)carbonyl)-2-methylpropyl)amino)-6,7-(1,2,3,4-tetrahydro-1,1,4,4-tetramethylbenzo)-1H-indol-3-yl)-2-oximidopropionate Edit
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Technology Process of ethyl (S)-3-(4-(methyl(1-(((phenylmethyl)oxy)carbonyl)-2-methylpropyl)amino)-6,7-(1,2,3,4-tetrahydro-1,1,4,4-tetramethylbenzo)-1H-indol-3-yl)-2-oximidopropionate

There total 11 articles about ethyl (S)-3-(4-(methyl(1-(((phenylmethyl)oxy)carbonyl)-2-methylpropyl)amino)-6,7-(1,2,3,4-tetrahydro-1,1,4,4-tetramethylbenzo)-1H-indol-3-yl)-2-oximidopropionate 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 10 steps
1: 99 percent / AlCl3 / 12 h / Heating
2: 57 percent / H2SO4, conc., HNO3, fum. / 1,2-dichloro-ethane / 2 h / 0 °C
3: 100 percent / Triton-B / dimethylsulfoxide / 12 h
4: 99 percent / cyclohexene / 10percent Pd/C / ethanol / 1 h / Heating
5: 95 percent / aq. NaHCO3 / tetrahydrofuran / 12 h / 0 deg C, warming to RT
6: 95 percent / Fe, HOAc / ethanol / 3 h / Heating
7: 78 percent / tris(triphenylphosphine)ruthenium dichloride / toluene / 3 h / Heating
8: 92 percent / LiAlH4 / tetrahydrofuran / 0.5 h / Heating
9: 93 percent / 2,6-lutidine / 1,2-dichloro-ethane / 12 h / Heating
10: 50 percent / Na2CO3 / CH2Cl2 / 12 h
With 2,6-dimethylpyridine; lithium aluminium tetrahydride; aluminium trichloride; tris(triphenylphosphine)ruthenium(II) chloride; sulfuric acid; nitric acid; N-benzyl-trimethylammonium hydroxide; iron; sodium hydrogencarbonate; sodium carbonate; acetic acid; cyclohexene; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide; 1,2-dichloro-ethane; toluene;
DOI:10.1021/jo00015a026
Guidance literature:
Multi-step reaction with 9 steps
1: 57 percent / H2SO4, conc., HNO3, fum. / 1,2-dichloro-ethane / 2 h / 0 °C
2: 100 percent / Triton-B / dimethylsulfoxide / 12 h
3: 99 percent / cyclohexene / 10percent Pd/C / ethanol / 1 h / Heating
4: 95 percent / aq. NaHCO3 / tetrahydrofuran / 12 h / 0 deg C, warming to RT
5: 95 percent / Fe, HOAc / ethanol / 3 h / Heating
6: 78 percent / tris(triphenylphosphine)ruthenium dichloride / toluene / 3 h / Heating
7: 92 percent / LiAlH4 / tetrahydrofuran / 0.5 h / Heating
8: 93 percent / 2,6-lutidine / 1,2-dichloro-ethane / 12 h / Heating
9: 50 percent / Na2CO3 / CH2Cl2 / 12 h
With 2,6-dimethylpyridine; lithium aluminium tetrahydride; tris(triphenylphosphine)ruthenium(II) chloride; sulfuric acid; nitric acid; N-benzyl-trimethylammonium hydroxide; iron; sodium hydrogencarbonate; sodium carbonate; acetic acid; cyclohexene; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; dimethyl sulfoxide; 1,2-dichloro-ethane; toluene;
DOI:10.1021/jo00015a026
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