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1H-Thieno[2,3-c]pyrazole-5-carboxylic acid, 3-[[4-(4-morpholinylmethyl)benzoyl]amino]-, 2-methyl-2-phenylhydrazide

Base Information Edit
  • Chemical Name:1H-Thieno[2,3-c]pyrazole-5-carboxylic acid, 3-[[4-(4-morpholinylmethyl)benzoyl]amino]-, 2-methyl-2-phenylhydrazide
  • CAS No.:909252-67-1
  • Molecular Formula:C25H26N6O3S
  • Molecular Weight:490.586
  • Hs Code.:
  • Mol file:909252-67-1.mol
1H-Thieno[2,3-c]pyrazole-5-carboxylic acid,
3-[[4-(4-morpholinylmethyl)benzoyl]amino]-, 2-methyl-2-phenylhydrazide

Synonyms:

Suppliers and Price of 1H-Thieno[2,3-c]pyrazole-5-carboxylic acid, 3-[[4-(4-morpholinylmethyl)benzoyl]amino]-, 2-methyl-2-phenylhydrazide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1H-Thieno[2,3-c]pyrazole-5-carboxylic acid, 3-[[4-(4-morpholinylmethyl)benzoyl]amino]-, 2-methyl-2-phenylhydrazide Edit
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Technology Process of 1H-Thieno[2,3-c]pyrazole-5-carboxylic acid, 3-[[4-(4-morpholinylmethyl)benzoyl]amino]-, 2-methyl-2-phenylhydrazide

There total 10 articles about 1H-Thieno[2,3-c]pyrazole-5-carboxylic acid, 3-[[4-(4-morpholinylmethyl)benzoyl]amino]-, 2-methyl-2-phenylhydrazide 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
1.1: triethylamine
2.1: isopentyl nitrite / N,N-dimethyl-formamide / 2.5 h / 60 - 70 °C
3.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 21 h / -5 - 25 °C
4.1: hydrazine / ethanol / 4 h / Heating / reflux
4.2: 4 h / 25 °C
5.1: trimethylaluminum / toluene / 1 h / 25 °C
5.2: 16 h / Heating / reflux
6.1: triethylamine / dichloromethane / 0.25 h / 25 °C
6.2: 4 h / 0 - 25 °C
7.1: potassium carbonate / tetrahydrofuran / 2 h / 25 °C
8.1: potassium carbonate / methanol / 0.05 h / 180 °C / Microwave irradiation
With trimethylaluminum; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; hydrazine; isopentyl nitrite; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;
Guidance literature:
Multi-step reaction with 7 steps
1.1: isopentyl nitrite / N,N-dimethyl-formamide / 2.5 h / 60 - 70 °C
2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 21 h / -5 - 25 °C
3.1: hydrazine / ethanol / 4 h / Heating / reflux
3.2: 4 h / 25 °C
4.1: trimethylaluminum / toluene / 1 h / 25 °C
4.2: 16 h / Heating / reflux
5.1: triethylamine / dichloromethane / 0.25 h / 25 °C
5.2: 4 h / 0 - 25 °C
6.1: potassium carbonate / tetrahydrofuran / 2 h / 25 °C
7.1: potassium carbonate / methanol / 0.05 h / 180 °C / Microwave irradiation
With trimethylaluminum; potassium carbonate; triethylamine; 3-chloro-benzenecarboperoxoic acid; hydrazine; isopentyl nitrite; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;
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