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1-(2-pyridinyl)-Cyclopentanecarbonitrile

Base Information Edit
  • Chemical Name:1-(2-pyridinyl)-Cyclopentanecarbonitrile
  • CAS No.:400727-04-0
  • Molecular Formula:C11H12N2
  • Molecular Weight:172.22600
  • Hs Code.:
  • Mol file:400727-04-0.mol
1-(2-pyridinyl)-Cyclopentanecarbonitrile

Synonyms:1-pyridin-2-yl-cyclopentanecarbonitrile;

Suppliers and Price of 1-(2-pyridinyl)-Cyclopentanecarbonitrile
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
  • Crysdot
  • 1-(2-Pyridinyl)cyclopentanecarbonitrile 95+%
  • 1g
  • $ 474.00
  • Alichem
  • 1-(Pyridin-2-yl)cyclopentanecarbonitrile
  • 1g
  • $ 464.63
  • Alichem
  • 1-(Pyridin-2-yl)cyclopentanecarbonitrile
  • 250mg
  • $ 197.76
Total 13 raw suppliers
Chemical Property of 1-(2-pyridinyl)-Cyclopentanecarbonitrile Edit
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:334.051oC at 760 mmHg 
  • PKA:5.65±0.19(Predicted) 
  • Flash Point:118.048oC 
  • PSA:36.68000 
  • Density:1.097g/cm3 
  • LogP:2.41698 
Purity/Quality:

97% *data from raw suppliers

1-(2-Pyridinyl)cyclopentanecarbonitrile 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 1-(2-pyridinyl)-Cyclopentanecarbonitrile

There total 1 articles about 1-(2-pyridinyl)-Cyclopentanecarbonitrile 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 sodium hydride; In diethyl ether; dimethyl sulfoxide; mineral oil; at 15 - 20 ℃; for 25h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 6 steps
1: water; hydrogenchloride / 16 h / 80 °C / Sealed tube
2: borane-THF / tetrahydrofuran / 6 h / 0 - 20 °C
3: triethylamine / dichloromethane / 2 h / 0 - 20 °C
4: potassium iodide / dimethyl sulfoxide / 5 h / 140 °C
5: ammonium chloride; trimethylaluminum / toluene / 14 h / 5 - 100 °C
6: sodium methylate / methanol / 16 h / 0 - 20 °C
With hydrogenchloride; borane-THF; water; trimethylaluminum; sodium methylate; ammonium chloride; triethylamine; potassium iodide; In tetrahydrofuran; methanol; dichloromethane; dimethyl sulfoxide; toluene;
Guidance literature:
Multi-step reaction with 7 steps
1: water; hydrogenchloride / 16 h / 80 °C / Sealed tube
2: borane-THF / tetrahydrofuran / 6 h / 0 - 20 °C
3: triethylamine / dichloromethane / 2 h / 0 - 20 °C
4: potassium iodide / dimethyl sulfoxide / 5 h / 140 °C
5: ammonium chloride; trimethylaluminum / toluene / 14 h / 5 - 100 °C
6: sodium methylate / methanol / 16 h / 0 - 20 °C
7: lithium hydroxide monohydrate / tetrahydrofuran; water / 16 h / Reflux
With hydrogenchloride; borane-THF; lithium hydroxide monohydrate; water; trimethylaluminum; sodium methylate; ammonium chloride; triethylamine; potassium iodide; In tetrahydrofuran; methanol; dichloromethane; water; dimethyl sulfoxide; toluene;
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