Benzonitrile, 4-[(1E)-2-(4-pyridinyl)ethenyl]-

Base Information

Chemical Name:Benzonitrile, 4-[(1E)-2-(4-pyridinyl)ethenyl]-
CAS No.:133792-94-6
Molecular Formula:C14H10N2
Molecular Weight:206.247
Hs Code.:
DSSTox Substance ID:DTXSID70391119

Synonyms:Benzonitrile, 4-[(1E)-2-(4-pyridinyl)ethenyl]-;133792-94-6;DTXSID70391119

Suppliers and Price of Benzonitrile, 4-[(1E)-2-(4-pyridinyl)ethenyl]-

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 Benzonitrile, 4-[(1E)-2-(4-pyridinyl)ethenyl]-

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:206.084398327
Heavy Atom Count:16
Complexity:272

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C=CC2=CC=NC=C2)C#N

Technology Process of Benzonitrile, 4-[(1E)-2-(4-pyridinyl)ethenyl]-

There total 4 articles about Benzonitrile, 4-[(1E)-2-(4-pyridinyl)ethenyl]- 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: 50.0%

: 108-89-4
picoline

: 105-07-7
4-cyanobenzaldehyde

: 133792-94-6
(E)-4-[2-(4-pyridyl)ethenyl]benzenecarbonitrile

Guidance literature:: In acetic anhydride; for 8h; Reflux;
DOI:10.1039/c7dt01648d

Reference yield:

: 874-86-2
4-cyanobenzyl chloride

: 133792-94-6
(E)-4-[2-(4-pyridyl)ethenyl]benzenecarbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran / 4 h / Reflux

2: sodium hydride / tetrahydrofuran / 1 h / Cooling with ice; Reflux

With sodium hydride; In tetrahydrofuran;
DOI:10.1002/poc.4246