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N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide

Base Information Edit
  • Chemical Name:N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide
  • CAS No.:1352740-91-0
  • Molecular Formula:C11H13BrINO2S
  • Molecular Weight:430.104
  • Hs Code.:
  • Mol file:1352740-91-0.mol
N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide

Synonyms:N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide

Suppliers and Price of N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide Edit
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Technology Process of N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide

There total 3 articles about N-allyl-N-(2-iodoethyl)-2-bromobenzenesulfonamide 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:
With sodium iodide; In acetone; at 60 ℃; for 4h; Inert atmosphere;
DOI:10.1002/anie.201105235
Guidance literature:
Multi-step reaction with 2 steps
1: triethylamine / dichloromethane / 0 - 20 °C
2: sodium iodide / acetone / 4 h / 60 °C / Inert atmosphere
With triethylamine; sodium iodide; In dichloromethane; acetone;
DOI:10.1002/anie.201105235
Guidance literature:
Multi-step reaction with 3 steps
1: lithium aluminium tetrahydride / tetrahydrofuran / 0 °C / Inert atmosphere
2: triethylamine / dichloromethane / 0 - 20 °C
3: sodium iodide / acetone / 4 h / 60 °C / Inert atmosphere
With lithium aluminium tetrahydride; triethylamine; sodium iodide; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1002/anie.201105235
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