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4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium

Base Information Edit
  • Chemical Name:4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium
  • CAS No.:639010-33-6
  • Molecular Formula:C17H14F3N3O2S*HNa
  • Molecular Weight:405.376
  • Hs Code.:
  • Mol file:639010-33-6.mol
4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium

Synonyms:4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium

Suppliers and Price of 4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium Edit
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Technology Process of 4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium

There total 3 articles about 4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide sodium 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: ethanol / Reflux
2: sodium hydroxide / water; ethanol / 0.08 h / 20 °C
With sodium hydroxide; In ethanol; water;
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium methylate / methanol; tert-butyl methyl ether / 20 °C / Inert atmosphere
1.2: 20 °C
2.1: ethanol / Reflux
3.1: sodium hydroxide / water; ethanol / 0.08 h / 20 °C
With sodium methylate; sodium hydroxide; In methanol; ethanol; tert-butyl methyl ether; water;
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