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{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

Base Information Edit
  • Chemical Name:{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester
  • CAS No.:105763-67-5
  • Molecular Formula:C22H33N3O6
  • Molecular Weight:435.521
  • Hs Code.:
  • Mol file:105763-67-5.mol
{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

Synonyms:{5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

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Chemical Property of {5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester Edit
Chemical Property:
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SDS file from LookChem

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Technology Process of {5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester

There total 6 articles about {5-[3-(Cyclohexyl-methyl-carbamoyl)-propoxy]-2-nitro-benzylamino}-acetic acid ethyl ester 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: aq. Na2CO3 / tetrahydrofuran / 1 h / Ambient temperature
2: NaBH3CN / ethanol / 3 h
With sodium cyanoborohydride; sodium carbonate; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00385a011
Guidance literature:
Multi-step reaction with 5 steps
1: 95 percent / K2CO3 / dimethylformamide / 1 h / 100 °C
2: 96 percent / aq. KOH / ethanol
3: oxalyl chloride / benzene; dimethylformamide / 1 h / Ambient temperature
4: aq. Na2CO3 / tetrahydrofuran / 1 h / Ambient temperature
5: NaBH3CN / ethanol / 3 h
With potassium hydroxide; oxalyl dichloride; sodium cyanoborohydride; sodium carbonate; potassium carbonate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a011
Guidance literature:
Multi-step reaction with 4 steps
1: 96 percent / aq. KOH / ethanol
2: oxalyl chloride / benzene; dimethylformamide / 1 h / Ambient temperature
3: aq. Na2CO3 / tetrahydrofuran / 1 h / Ambient temperature
4: NaBH3CN / ethanol / 3 h
With potassium hydroxide; oxalyl dichloride; sodium cyanoborohydride; sodium carbonate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; benzene;
DOI:10.1021/jm00385a011
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