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Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide

Base Information Edit
  • Chemical Name:Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide
  • CAS No.:1268830-77-8
  • Molecular Formula:C9H12ClFN2O2S
  • Molecular Weight:266.724
  • Hs Code.:
  • Mol file:1268830-77-8.mol
Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide

Synonyms:Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide

Suppliers and Price of Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 2 raw suppliers
Chemical Property of Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
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Technology Process of Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide

There total 6 articles about Ν-(2-chloro-3-amino-4-fluorophenyl)-1-propyl sulfonamide 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:
2-chloro-6-fluoro-3-(propylsulfonamido)benzoic acid; With diphenyl phosphoryl azide; triethylamine; In tetrahydrofuran; at 20 - 80 ℃; for 5h; Inert atmosphere;
With water; In tetrahydrofuran; at 80 ℃; for 2h;
DOI:10.1021/jm300016v
Guidance literature:
Multi-step reaction with 4 steps
1.1: hydroxylamine hydrochloride; triethylamine / ethanol; water / 18 h / Reflux; Inert atmosphere
2.1: triethylamine / dichloromethane / 1.33 h / 0 °C / Inert atmosphere
2.2: 2 h / 20 °C
3.1: water; potassium hydroxide / tetrahydrofuran; water / 2 h / Reflux; Inert atmosphere
4.1: diphenyl phosphoryl azide; triethylamine / tetrahydrofuran / 5 h / 20 - 80 °C / Inert atmosphere
4.2: 2 h / 80 °C
With diphenyl phosphoryl azide; hydroxylamine hydrochloride; water; triethylamine; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1021/jm300016v
Guidance literature:
Multi-step reaction with 6 steps
1.1: toluene-4-sulfonic acid / toluene / 1 h / Reflux; Inert atmosphere
2.1: n-butyllithium / tetrahydrofuran / 1.33 h / -78 °C / Inert atmosphere
2.2: 2.5 h / -78 °C / Inert atmosphere
3.1: hydroxylamine hydrochloride; triethylamine / ethanol; water / 18 h / Reflux; Inert atmosphere
4.1: triethylamine / dichloromethane / 1.33 h / 0 °C / Inert atmosphere
4.2: 2 h / 20 °C
5.1: water; potassium hydroxide / tetrahydrofuran; water / 2 h / Reflux; Inert atmosphere
6.1: diphenyl phosphoryl azide; triethylamine / tetrahydrofuran / 5 h / 20 - 80 °C / Inert atmosphere
6.2: 2 h / 80 °C
With n-butyllithium; diphenyl phosphoryl azide; hydroxylamine hydrochloride; water; toluene-4-sulfonic acid; triethylamine; potassium hydroxide; In tetrahydrofuran; ethanol; dichloromethane; water; toluene;
DOI:10.1021/jm300016v
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