2-(6-Methoxypyridin-2-yl)azepane

Base Information

Chemical Name:2-(6-Methoxypyridin-2-yl)azepane
CAS No.:5012-77-1
Molecular Formula:C₁₇H₃₁N₃
Molecular Weight:277.453
Hs Code.:
DSSTox Substance ID:DTXSID20411154

Synonyms:5012-77-1;2-(6-methoxypyridin-2-yl)azepane;DTXSID20411154

Suppliers and Price of 2-(6-Methoxypyridin-2-yl)azepane

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 1 raw suppliers

Chemical Property of 2-(6-Methoxypyridin-2-yl)azepane

Chemical Property:

Vapor Pressure:0.000387mmHg at 25°C
Boiling Point:317.4°Cat760mmHg
Flash Point:145.7°C
Density:1.023g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:206.141913202
Heavy Atom Count:15
Complexity:187

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC(=N1)C2CCCCCN2

Technology Process of 2-(6-Methoxypyridin-2-yl)azepane

There total 2 articles about 2-(6-Methoxypyridin-2-yl)azepane 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:

: 110-89-4
piperidine

: 5012-77-1
Cyclohexyl-(di-piperidin-1-yl-methylene)-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / ethyldiisopropylamine / CH₂Cl₂ / 24 h / 40 °C

2: 1.) oxalyl chloride / 1.) DME, 60 deg C, 12 h, 2.) MeCN, reflux, 24 h

With oxalyl dichloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1039/a800453f