2,6-Divinylpyridine

Base Information

Chemical Name:2,6-Divinylpyridine
CAS No.:1124-74-9
Molecular Formula:C9H9N
Molecular Weight:131.177
Hs Code.:
DSSTox Substance ID:DTXSID60478983
Nikkaji Number:J786.032C
Wikidata:Q82312781

Synonyms:2,6-divinylpyridine;1124-74-9;SCHEMBL6273480;DTXSID60478983

Suppliers and Price of 2,6-Divinylpyridine

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 2 raw suppliers

Chemical Property of 2,6-Divinylpyridine

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:131.073499291
Heavy Atom Count:10
Complexity:115

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CC1=NC(=CC=C1)C=C

Technology Process of 2,6-Divinylpyridine

There total 1 articles about 2,6-Divinylpyridine 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:

: 108-48-5
2,6-dimethylpyridine

: 50-00-0,30525-89-4,61233-19-0
formaldehyd

: 1122-70-9
2-methyl-6-vinylpyridine

: 1124-74-9
2,6-divinylpyridine

Guidance literature:: HZSM-5 (SiO₂/Al₂O₃=30), cesium nitrate and water mixed, dried and calcined; at 300 ℃; for 6h;

Reference yield: 85.0%

: 1124-74-9
2,6-divinylpyridine

: 5281-18-5
benzaldehyde, hydrazone

: 1101197-16-3
2,6-bis(3-phenylpropyl)pyridine

Guidance literature:: With [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; 1,2-bis(dimethylphosphanyl)ethane; lithium tert-butoxide; In tetrahydrofuran; at 80 ℃; for 12h; regioselective reaction; Inert atmosphere;
DOI:10.1039/d0sc06586b