Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester

Base Information Edit
  • Chemical Name:trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester
  • CAS No.:1436862-11-1
  • Molecular Formula:C7H12N4O6S
  • Molecular Weight:280.261
  • Hs Code.:
  • Mol file:1436862-11-1.mol
trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester

Synonyms:trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester

Suppliers and Price of trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester
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
Total 0 raw suppliers
Chemical Property of trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester

There total 1 articles about trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester 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 11 steps
1.1: hydrogenchloride / 3 h / Reflux
2.1: triethylamine / tetrahydrofuran / 2.17 h / 10 - 20 °C / Cooling with ice
3.1: 2,6-dimethylpyridine; trifluoromethylsulfonic anhydride / acetonitrile / 0.67 h / -36 - -30 °C
3.2: 48 h / -32 - 4 °C
4.1: hydrogenchloride / methanol / 72 h / Reflux
5.1: potassium carbonate / ethyl acetate; water
6.1: triethylamine / acetonitrile / 0.33 h / 2 - 5 °C / Cooling with ice
6.2: 10 h / 20 °C
7.1: water; lithium hydroxide / tetrahydrofuran / 2.17 h / 2 - 4.9 °C
8.1: triethylamine; isobutyl chloroformate / tetrahydrofuran / 0.25 h / 0 °C / Cooling with ice
8.2: 1.5 h / 0 - 20 °C
9.1: palladium 10% on activated carbon; hydrogen / water; methanol / 0.92 h / 20 °C
10.1: sulfur trioxide pyridine complex / pyridine / 20 °C
10.2: 0.25 h
11.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C
With 2,6-dimethylpyridine; hydrogenchloride; trifluoromethylsulfonic anhydride; palladium 10% on activated carbon; water; hydrogen; sulfur trioxide pyridine complex; potassium carbonate; triethylamine; trifluoroacetic acid; lithium hydroxide; isobutyl chloroformate; In tetrahydrofuran; pyridine; methanol; dichloromethane; water; ethyl acetate; acetonitrile;
Guidance literature:
3-[(tert-butoxycarbonyl)amino]-3-(3,4-bis-benzyloxyphenyl)propionic acid; With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h;
trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 17h;
Guidance literature:
trans-sulfuric acid mono-[2-hydrazinocarbonyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]ester; ortho-anisaldehyde; With N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; at 25 ℃; for 16h;
tetrabutylammonium acetate; In tetrahydrofuran; at 25 ℃; for 22h;
Refernces Edit
Post RFQ for Price