2-(2-Aminobenzyl)pyridine

Base Information

Chemical Name:2-(2-Aminobenzyl)pyridine
CAS No.:53114-00-4
Molecular Formula:C₁₂H₁₂N₂
Molecular Weight:184.241
Hs Code.:
European Community (EC) Number:898-533-4

Synonyms:2-[(pyridin-2-yl)methyl]aniline;53114-00-4;2-(2-aminobenzyl)pyridine;2-(pyridin-2-ylmethyl)aniline;SCHEMBL7112576;AKOS014777297;CS-0238027;EN300-189139

Suppliers and Price of 2-(2-Aminobenzyl)pyridine

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-(2-Aminobenzyl)pyridine

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:184.100048391
Heavy Atom Count:14
Complexity:170

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)CC2=CC=CC=N2)N

Technology Process of 2-(2-Aminobenzyl)pyridine

There total 10 articles about 2-(2-Aminobenzyl)pyridine 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:

Reference yield: 41.0%

: 115177-61-2
2-(o-azidobenzyl)pyridine

: 53114-00-4
2-(2-aminobenzyl)pyridine

: 25398-94-1
3H-1,2-diazepino<1,7-a>indole

Guidance literature:: In various solvent(s); at 190 - 200 ℃; for 5h;
DOI:10.1016/S0040-4039(00)80129-X

Reference yield:

: 109-04-6
2-bromo-pyridine

: 53114-00-4
2-(2-aminobenzyl)pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) butyl-lithium / 1.) ether, -70 deg C, 10 min, 2.) ether, -70 deg C, 30 min, RT, 2 h

2: 87 percent / H₂ / 10percent Pd-C / aq. ethanol

3: 1.) hydroiodic acid, 2.) sodium metabisulphite, 50percent sodium hydroxide / 1.) reflux, 5 h, 2.) H₂O, 100 deg C, 5 min

With sodium hydroxide; sodium disulfite; n-butyllithium; hydrogen iodide; hydrogen; palladium on activated charcoal; In ethanol;

Reference yield:

: 115177-58-7
(2-nitrophenyl)(pyridin-2-yl)methanol

: 53114-00-4
2-(2-aminobenzyl)pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / H₂ / 10percent Pd-C / aq. ethanol

2: 1.) hydroiodic acid, 2.) sodium metabisulphite, 50percent sodium hydroxide / 1.) reflux, 5 h, 2.) H₂O, 100 deg C, 5 min

With sodium hydroxide; sodium disulfite; hydrogen iodide; hydrogen; palladium on activated charcoal; In ethanol;