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3-amino-4-(1-piperidinyl)-benzonitrile

Base Information
  • Chemical Name:3-amino-4-(1-piperidinyl)-benzonitrile
  • CAS No.:27429-67-0
  • Molecular Formula:C12H15N3
  • Molecular Weight:201.271
  • Hs Code.:
  • Mol file:27429-67-0.mol
3-amino-4-(1-piperidinyl)-benzonitrile

Synonyms:3-Amino-4-piperidinobenzonitril;3-Amino-4-piperidino-benzonitril;3-Amino-4-piperidin-1-yl-benzonitrile;

Suppliers and Price of 3-amino-4-(1-piperidinyl)-benzonitrile
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
  • Crysdot
  • 3-Amino-4-(piperidin-1-yl)benzonitrile 97%
  • 1g
  • $ 474.00
  • A1 Biochem Labs
  • 3-Amino-4-(1-piperidinyl)-benzonitrile 95%
  • 5 g
  • $ 1100.00
Total 6 raw suppliers
Chemical Property of 3-amino-4-(1-piperidinyl)-benzonitrile
Chemical Property:
  • Melting Point:56 °C 
  • PSA:53.05000 
  • LogP:2.77698 
Purity/Quality:

98%+ *data from raw suppliers

3-Amino-4-(piperidin-1-yl)benzonitrile 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 3-amino-4-(1-piperidinyl)-benzonitrile

There total 6 articles about 3-amino-4-(1-piperidinyl)-benzonitrile 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 10% Pt/activated carbon; hydrogen; In ethanol; at 25 ℃;
Guidance literature:
Multi-step reaction with 2 steps
1: sodium acetate; alcohol
2: tin dichloride; fuming hydrochloric acid
With hydrogenchloride; ethanol; sodium acetate; tin(ll) chloride;
Guidance literature:
Multi-step reaction with 2 steps
1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 0 - 80 °C
2: zinc; ammonium chloride / ethanol / 16 h / Inert atmosphere; Reflux
With potassium carbonate; ammonium chloride; zinc; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.bioorg.2021.105244
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