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Acetamide, N-[4-bromo-2-[[3-bromo-1-(phenylsulfonyl)-1H-indol-2-yl]methyl]-5-meth oxyphenyl]-

Base Information Edit
  • Chemical Name:Acetamide, N-[4-bromo-2-[[3-bromo-1-(phenylsulfonyl)-1H-indol-2-yl]methyl]-5-meth oxyphenyl]-
  • CAS No.:565227-62-5
  • Molecular Formula:C24H20Br2N2O4S
  • Molecular Weight:592.308
  • Hs Code.:
  • Mol file:565227-62-5.mol
Acetamide,
N-[4-bromo-2-[[3-bromo-1-(phenylsulfonyl)-1H-indol-2-yl]methyl]-5-meth
oxyphenyl]-

Synonyms:

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Chemical Property of Acetamide, N-[4-bromo-2-[[3-bromo-1-(phenylsulfonyl)-1H-indol-2-yl]methyl]-5-meth oxyphenyl]- Edit
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MSDS Files:

SDS file from LookChem

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Technology Process of Acetamide, N-[4-bromo-2-[[3-bromo-1-(phenylsulfonyl)-1H-indol-2-yl]methyl]-5-meth oxyphenyl]-

There total 2 articles about Acetamide, N-[4-bromo-2-[[3-bromo-1-(phenylsulfonyl)-1H-indol-2-yl]methyl]-5-meth oxyphenyl]- 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: 78.4 percent / aq. potassium carbonate / acetonitrile / 5 h / Heating
2: 76 percent / BF3*Et2O; MgSO4 / CHCl3 / 3 h / Heating
With boron trifluoride diethyl etherate; magnesium sulfate; potassium carbonate; In chloroform; acetonitrile;
DOI:10.1081/SCC-120021513
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