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cis-3-[(tert-butoxycarbonyl)(methyl)amino]cyclobutyl methanesulfonate

Base Information Edit
  • Chemical Name:cis-3-[(tert-butoxycarbonyl)(methyl)amino]cyclobutyl methanesulfonate
  • CAS No.:1033718-11-4
  • Molecular Formula:C11H21NO5S
  • Molecular Weight:279.357
  • Hs Code.:
  • Mol file:1033718-11-4.mol
cis-3-[(tert-butoxycarbonyl)(methyl)amino]cyclobutyl methanesulfonate

Synonyms:

Suppliers and Price of cis-3-[(tert-butoxycarbonyl)(methyl)amino]cyclobutyl methanesulfonate
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • TERT-BUTYL N-METHYL-N-[(1S,3S)-3-(METHANESULFONYLOXY)CYCLOBUTYL]CARBAMATE 95.00%
  • 5MG
  • $ 456.64
Total 4 raw suppliers
Chemical Property of cis-3-[(tert-butoxycarbonyl)(methyl)amino]cyclobutyl methanesulfonate Edit
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

TERT-BUTYL N-METHYL-N-[(1S,3S)-3-(METHANESULFONYLOXY)CYCLOBUTYL]CARBAMATE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of cis-3-[(tert-butoxycarbonyl)(methyl)amino]cyclobutyl methanesulfonate

There total 6 articles about cis-3-[(tert-butoxycarbonyl)(methyl)amino]cyclobutyl methanesulfonate 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:
tert-butyl (cis-3-hydroxycyclobutyl)methylcarbamate; With triethylamine; In dichloromethane; at -30 ℃;
methanesulfonyl chloride; In dichloromethane; at 20 ℃; for 1.16667h;
Guidance literature:
Multi-step reaction with 6 steps
1.1: ozone / methanol; dichloromethane / -78 °C / Inert atmosphere
2.1: L-Selectride / tetrahydrofuran / 2.5 h / -72 - 20 °C
3.1: pyridine / 20 °C
4.1: sodium hydride / mineral oil; tetrahydrofuran / 0.5 h / 20 °C
4.2: 0 - 20 °C
5.1: tetrabutyl ammonium fluoride; pyridine / 2 h / 20 °C
6.1: triethylamine / dichloromethane / -30 °C
6.2: 1.17 h / 20 °C
With pyridine; tetrabutyl ammonium fluoride; L-Selectride; sodium hydride; ozone; triethylamine; In tetrahydrofuran; methanol; dichloromethane; mineral oil;
Guidance literature:
Multi-step reaction with 5 steps
1.1: L-Selectride / tetrahydrofuran / 2.5 h / -72 - 20 °C
2.1: pyridine / 20 °C
3.1: sodium hydride / mineral oil; tetrahydrofuran / 0.5 h / 20 °C
3.2: 0 - 20 °C
4.1: tetrabutyl ammonium fluoride; pyridine / 2 h / 20 °C
5.1: triethylamine / dichloromethane / -30 °C
5.2: 1.17 h / 20 °C
With pyridine; tetrabutyl ammonium fluoride; L-Selectride; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane; mineral oil;
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