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(-)-feniramidol

Base Information Edit
  • Chemical Name:(-)-feniramidol
  • CAS No.:92842-83-6
  • Molecular Formula:C13H14N2O
  • Molecular Weight:214.267
  • Hs Code.:
  • UNII:B3SJ811M2N
  • Mol file:92842-83-6.mol
(-)-feniramidol

Synonyms:(-)-feniramidol

Suppliers and Price of (-)-feniramidol
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
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  • price
Total 0 raw suppliers
Chemical Property of (-)-feniramidol Edit
Chemical Property:
  • XLogP3:2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:214.110613074
  • Heavy Atom Count:16
  • Complexity:192
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(CNC2=CC=CC=N2)O
  • Isomeric SMILES:C1=CC=C(C=C1)[C@H](CNC2=CC=CC=N2)O
Technology Process of (-)-feniramidol

There total 6 articles about (-)-feniramidol 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:
2-aminopyridine; With lithium amide; In N,N-dimethyl-formamide; at 10 - 80 ℃; for 0.5 - 1h;
(S)-styrene oxide; In N,N-dimethyl-formamide; at 90 - 100 ℃; for 1.66 - 2h;
With water; In toluene; at 60 ℃; for 0.166667 - 0.333333h; Product distribution / selectivity;
Guidance literature:
With sodium hydrogencarbonate; In water; at 20 - 50 ℃; for 1h; pH=4 - > 8; Product distribution / selectivity;
Guidance literature:
With triethylamine; N-ethyl-N,N-diisopropylamine; at 158 - 165 ℃; Microwave irradiation;
DOI:10.1002/ejoc.201501596
Refernces Edit
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