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2-Azabicyclo[2.2.1]heptane-2-butanenitrile

Base Information Edit
  • Chemical Name:2-Azabicyclo[2.2.1]heptane-2-butanenitrile
  • CAS No.:947263-49-2
  • Molecular Formula:C10H16N2
  • Molecular Weight:164.25
  • Hs Code.:
  • Mol file:947263-49-2.mol
2-Azabicyclo[2.2.1]heptane-2-butanenitrile

Synonyms:2-Azabicyclo[2.2.1]heptane-2-butanenitrile

Suppliers and Price of 2-Azabicyclo[2.2.1]heptane-2-butanenitrile
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
  • AccelPharmtech
  • 2-Azabicyclo[2.2.1]heptane-2-butanenitrile 97.00%
  • 25G
  • $ 6000.00
  • AccelPharmtech
  • 2-Azabicyclo[2.2.1]heptane-2-butanenitrile 97.00%
  • 5G
  • $ 3230.00
  • AccelPharmtech
  • 2-Azabicyclo[2.2.1]heptane-2-butanenitrile 97.00%
  • 1G
  • $ 1890.00
Total 0 raw suppliers
Chemical Property of 2-Azabicyclo[2.2.1]heptane-2-butanenitrile Edit
Chemical Property:
  • PSA:27.03000 
  • LogP:1.71238 
Purity/Quality:

2-Azabicyclo[2.2.1]heptane-2-butanenitrile 97.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-Azabicyclo[2.2.1]heptane-2-butanenitrile

There total 1 articles about 2-Azabicyclo[2.2.1]heptane-2-butanenitrile 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 potassium carbonate; potassium iodide; In butan-1-ol; for 20h; Heating;
DOI:10.1021/jm0701627
Guidance literature:
Multi-step reaction with 2 steps
1: 76 percent / LiAlH4 / diethyl ether / 1 h / 0 °C
2: 0.76 g / triethylamine / tetrahydrofuran / 2 h
With lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; diethyl ether;
DOI:10.1021/jm0701627
Guidance literature:
Multi-step reaction with 2 steps
1: 76 percent / LiAlH4 / diethyl ether / 1 h / 0 °C
2: 0.94 g / triethylamine / tetrahydrofuran / 2 h
With lithium aluminium tetrahydride; triethylamine; In tetrahydrofuran; diethyl ether;
DOI:10.1021/jm0701627
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