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7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide

Base Information Edit
  • Chemical Name:7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide
  • CAS No.:864961-12-6
  • Molecular Formula:C17H18FNO3S2
  • Molecular Weight:367.465
  • Hs Code.:
  • Mol file:864961-12-6.mol
7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide

Synonyms:7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide

Suppliers and Price of 7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide Edit
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Technology Process of 7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide

There total 10 articles about 7-oxo-4,5,6,7-tetrahydro-benzo[b]thiophene-3-sulfonic acid [2-(4-fluorophenyl)-ethyl]-methyl-amide 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: hydrogen / 5%-palladium/activated carbon / methanol / 50 °C
2: triethylamine / tetrahydrofuran / 1 h / 0 - 20 °C
With hydrogen; triethylamine; 5%-palladium/activated carbon; In tetrahydrofuran; methanol;
Guidance literature:
Multi-step reaction with 3 steps
1: lithium aluminium tetrahydride / tetrahydrofuran / 1 h
2: hydrogen / 5%-palladium/activated carbon / methanol / 50 °C
3: triethylamine / tetrahydrofuran / 1 h / 0 - 20 °C
With lithium aluminium tetrahydride; hydrogen; triethylamine; 5%-palladium/activated carbon; In tetrahydrofuran; methanol;
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