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3-{[5-(biphenyl-4-yl)-6-chloro-1H-benzimidazol-2-yl]oxy}cyclopentane carboxylic acid

Base Information
  • Chemical Name:3-{[5-(biphenyl-4-yl)-6-chloro-1H-benzimidazol-2-yl]oxy}cyclopentane carboxylic acid
  • CAS No.:1332706-64-5
  • Molecular Formula:C25H21ClN2O3
  • Molecular Weight:432.906
  • Hs Code.:
3-{[5-(biphenyl-4-yl)-6-chloro-1H-benzimidazol-2-yl]oxy}cyclopentane carboxylic acid

Synonyms:3-{[5-(biphenyl-4-yl)-6-chloro-1H-benzimidazol-2-yl]oxy}cyclopentane carboxylic acid

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Chemical Property of 3-{[5-(biphenyl-4-yl)-6-chloro-1H-benzimidazol-2-yl]oxy}cyclopentane carboxylic acid
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Technology Process of 3-{[5-(biphenyl-4-yl)-6-chloro-1H-benzimidazol-2-yl]oxy}cyclopentane carboxylic acid

There total 10 articles about 3-{[5-(biphenyl-4-yl)-6-chloro-1H-benzimidazol-2-yl]oxy}cyclopentane carboxylic 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:
ethyl 3-{[5-(biphenyl-4-yl)-6-chloro-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-benzimidazol-2-yl]oxy}cyclopentanecarboxylate; With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 80 ℃; for 5.5h;
With water; sodium hydroxide; In methanol; at 20 ℃;
With hydrogenchloride; In water; pH=1;
Guidance literature:
Multi-step reaction with 9 steps
1.1: acetic acid; N-iodo-succinimide / 50 °C
2.1: ammonium chloride; iron / ethanol; water / 50 °C / Inert atmosphere
3.1: potassium hydroxide / ethanol / 3 h / Reflux
4.1: potassium carbonate / acetone / 0 - 20 °C
5.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.17 h / 20 °C
6.1: potassium phosphate / tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; water / 5 h / 100 °C
7.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 5 h / 20 °C
8.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 80 °C
9.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 5.5 h / 80 °C
9.2: 20 °C
9.3: pH 1
With potassium phosphate; N-iodo-succinimide; tetrabutyl ammonium fluoride; iron; potassium carbonate; ammonium chloride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; potassium hydroxide; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
Guidance literature:
Multi-step reaction with 8 steps
1.1: ammonium chloride; iron / ethanol; water / 50 °C / Inert atmosphere
2.1: potassium hydroxide / ethanol / 3 h / Reflux
3.1: potassium carbonate / acetone / 0 - 20 °C
4.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.17 h / 20 °C
5.1: potassium phosphate / tetrakis(triphenylphosphine) palladium(0) / 1,4-dioxane; water / 5 h / 100 °C
6.1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 5 h / 20 °C
7.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 80 °C
8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 5.5 h / 80 °C
8.2: 20 °C
8.3: pH 1
With potassium phosphate; tetrabutyl ammonium fluoride; iron; potassium carbonate; ammonium chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; potassium hydroxide; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
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