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tert-butyl N-isopropyl-N-methylsulfamoylcarbamate

Base Information
  • Chemical Name:tert-butyl N-isopropyl-N-methylsulfamoylcarbamate
  • CAS No.:958002-25-0
  • Molecular Formula:C9H20N2O4S
  • Molecular Weight:252.335
  • Hs Code.:
tert-butyl N-isopropyl-N-methylsulfamoylcarbamate

Synonyms:

Suppliers and Price of tert-butyl N-isopropyl-N-methylsulfamoylcarbamate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • N-[[Methyl(1-methylethyl)amino]sulfonyl]-carbamicAcid1,1-DimethylethylEster
  • 10mg
  • $ 100.00
Total 0 raw suppliers
Chemical Property of tert-butyl N-isopropyl-N-methylsulfamoylcarbamate
Chemical Property:
Purity/Quality:

N-[[Methyl(1-methylethyl)amino]sulfonyl]-carbamicAcid1,1-DimethylethylEster *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses N-[[Methyl(1-methylethyl)amino]sulfonyl]-carbamic Acid 1,1-Dimethylethyl Ester is an intermediate in the synthesis of unlabeled Saflufenacil-d7 (S081802). Saflufenacil-d7 is the labeled version of Saflufenacil (S081800), which is a herbicide of the pyrimidinedione chemical class used for the preplant burndown and selective preemergence dicot weed control in different field crops. It was found to inhibit protoporphyrinogen IX oxidase (PPO) enzyme.
Technology Process of tert-butyl N-isopropyl-N-methylsulfamoylcarbamate

There total 2 articles about tert-butyl N-isopropyl-N-methylsulfamoylcarbamate 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:
isocyanate de chlorosulfonyle; tert-butyl alcohol; In dichloromethane; at 0 ℃;
N-methylpropan-2-amine; With triethylamine; In dichloromethane; at 0 - 20 ℃;
Guidance literature:
With triethylamine; In dichloromethane; at 20 ℃; for 2h;
Guidance literature:
With hydrogenchloride; water; at 20 ℃; for 2h; Product distribution / selectivity;
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