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p-Toluol-(-N-carbethoxy)-iminosulfonsaeurechlorid

Base Information Edit
  • Chemical Name:p-Toluol-(-N-carbethoxy)-iminosulfonsaeurechlorid
  • CAS No.:93506-31-1
  • Molecular Formula:C10H12ClNO3S
  • Molecular Weight:261.729
  • Hs Code.:
  • Mol file:93506-31-1.mol
p-Toluol-(-N-carbethoxy)-iminosulfonsaeurechlorid

Synonyms:p-Toluol-(-N-carbethoxy)-iminosulfonsaeurechlorid

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of p-Toluol-(-N-carbethoxy)-iminosulfonsaeurechlorid Edit
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Technology Process of p-Toluol-(-N-carbethoxy)-iminosulfonsaeurechlorid

There total 6 articles about p-Toluol-(-N-carbethoxy)-iminosulfonsaeurechlorid 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 4 steps
1.1: thionyl chloride / dichloromethane / 3 h / 0 - 20 °C
2.1: triethylamine / 20 °C
3.1: lithium hexamethyldisilazane / tetrahydrofuran / -78 °C
3.2: 20 °C
4.1: N-chloro-succinimide / 2 h / 20 °C
With N-chloro-succinimide; thionyl chloride; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane;
DOI:10.1021/acsmedchemlett.9b00285
Guidance literature:
Multi-step reaction with 3 steps
1.1: triethylamine / 20 °C
2.1: lithium hexamethyldisilazane / tetrahydrofuran / -78 °C
2.2: 20 °C
3.1: N-chloro-succinimide / 2 h / 20 °C
With N-chloro-succinimide; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran;
DOI:10.1021/acsmedchemlett.9b00285
Guidance literature:
With N-chloro-succinimide; at 20 ℃; for 2h;
DOI:10.1021/acsmedchemlett.9b00285
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