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Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate

Base Information
  • Chemical Name:Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate
  • CAS No.:143619-67-4
  • Molecular Formula:C14H19NO2
  • Molecular Weight:233.31
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10569052
  • Wikidata:Q82455753
Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate

Synonyms:143619-67-4;Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate;DTXSID10569052

Suppliers and Price of Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate
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
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  • price
Total 1 raw suppliers
Chemical Property of Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate
Chemical Property:
  • XLogP3:3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:233.141578849
  • Heavy Atom Count:17
  • Complexity:259
Purity/Quality:

99.90% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(=O)C1(CCCCC1)C2=CN=CC=C2
Technology Process of Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate

There total 1 articles about Ethyl 1-(pyridin-3-yl)cyclohexane-1-carboxylate 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 tert-butylate; Yield given. Multistep reaction; 1.) DMF, RT, 0.5 h, 2.) DMF, RT, 4 h;
DOI:10.1021/jm00098a004
Guidance literature:
With sodium hydroxide; In methanol; for 48h; Ambient temperature;
DOI:10.1021/jm00098a004
Guidance literature:
Multi-step reaction with 2 steps
1: 36 percent / aq. NaOH / methanol / 48 h / Ambient temperature
2: SOCl2, DMF / 1.5 h / Heating
With sodium hydroxide; thionyl chloride; N,N-dimethyl-formamide; In methanol;
DOI:10.1021/jm00098a004
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