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2-Phenyl-1-pyridin-2-ylethanamine

Base Information
  • Chemical Name:2-Phenyl-1-pyridin-2-ylethanamine
  • CAS No.:16273-81-7
  • Molecular Formula:C13H14N2
  • Molecular Weight:198.268
  • Hs Code.:
  • European Community (EC) Number:837-129-4
  • Nikkaji Number:J2.456.907A
2-Phenyl-1-pyridin-2-ylethanamine

Synonyms:2-phenyl-1-pyridin-2-ylethanamine;2-phenyl-1-(pyridin-2-yl)ethan-1-amine;16273-81-7;SCHEMBL5570274;UVVZCVILTRYDBS-UHFFFAOYSA-N;alpha-Benzyl-2-pyridinemethaneamine;1-(2-pyridinyl)-2-phenylethylamine;(2-phenyl-1-pyridin-2-ylethyl)amine;AKOS010036703;CS-0263683;EN300-88865;E88020

Suppliers and Price of 2-Phenyl-1-pyridin-2-ylethanamine
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
Total 4 raw suppliers
Chemical Property of 2-Phenyl-1-pyridin-2-ylethanamine
Chemical Property:
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:198.115698455
  • Heavy Atom Count:15
  • Complexity:175
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CC(C2=CC=CC=N2)N
Technology Process of 2-Phenyl-1-pyridin-2-ylethanamine

There total 6 articles about 2-Phenyl-1-pyridin-2-ylethanamine 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 boron trifluoride diethyl etherate; In ethanol; at 140 ℃; for 32h; Schlenk technique; Inert atmosphere; Sealed tube;
DOI:10.1039/c7cc08512e
Guidance literature:
Multi-step reaction with 3 steps
1: 4A molecular sieve / CH2Cl2 / 5 h / Ambient temperature
2: KOH, TBAB / CH2Cl2 / 6 h / 50 °C
3: 2N aq. HCl / ethanol / 1 h / Ambient temperature
With hydrogenchloride; potassium hydroxide; 4 A molecular sieve; tetrabutylammomium bromide; In ethanol; dichloromethane;
DOI:10.1080/00397919208021301
Guidance literature:
With hydrogenchloride; In ethanol; for 1h; Yield given; Ambient temperature;
DOI:10.1080/00397919208021301
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