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cis-2-AMinocyclopentanecarbonitrile

Base Information
  • Chemical Name:cis-2-AMinocyclopentanecarbonitrile
  • CAS No.:874293-75-1
  • Molecular Formula:C6H10N2
  • Molecular Weight:110.159
  • Hs Code.:
  • Mol file:874293-75-1.mol
cis-2-AMinocyclopentanecarbonitrile

Synonyms:

Suppliers and Price of cis-2-AMinocyclopentanecarbonitrile
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
  • cis-2-Aminocyclopentanecarbonitrile
  • 100mg
  • $ 165.00
  • Matrix Scientific
  • cis-2-Aminocyclopentane-1-carbonitrile 95+%
  • 1g
  • $ 1848.00
  • J&W Pharmlab
  • cis-2-Amino-cyclopentanecarbonitrile 97%
  • 500mg
  • $ 998.00
  • Crysdot
  • cis-2-Aminocyclopentanecarbonitrile 95+%
  • 1g
  • $ 880.00
  • Chemenu
  • cis-2-Aminocyclopentane-1-carbonitrile 95%
  • 1g
  • $ 830.00
  • AK Scientific
  • cis-2-Aminocyclopentane-1-carbonitrile
  • 1g
  • $ 2544.00
Total 7 raw suppliers
Chemical Property of cis-2-AMinocyclopentanecarbonitrile
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

cis-2-Aminocyclopentanecarbonitrile *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses cis-2-Aminocyclopentanecarbonitrile is used in the preparation of novel 8-oxo-pyridooyrimidine Jak1/2 inhibitors. Also used in the synthesis of alicyclic β-amino nitriles.
Technology Process of cis-2-AMinocyclopentanecarbonitrile

There total 9 articles about cis-2-AMinocyclopentanecarbonitrile 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 hydrogenchloride; sodium tetrahydroborate; In methanol; for 3h;
DOI:10.1139/v99-216
Guidance literature:
With sodium tris(acetoxy)borohydride; acetic acid; at 20 ℃; for 3h;
DOI:10.1021/jf062845l
Guidance literature:
Multi-step reaction with 2 steps
1: 86 percent / NaH / tetrahydrofuran
2: 65 percent / NaHB(OAc)3; acetic acid / 3 h / 20 °C
With sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; In tetrahydrofuran;
DOI:10.1021/jf062845l
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