2-Phenylethene-1,1,2-tricarbonitrile

Base Information

Chemical Name:2-Phenylethene-1,1,2-tricarbonitrile
CAS No.:4364-80-1
Molecular Formula:C11H5 N3
Molecular Weight:179.181
Hs Code.:
NSC Number:142326
DSSTox Substance ID:DTXSID70301319
Nikkaji Number:J868.652A

Synonyms:2-phenylethene-1,1,2-tricarbonitrile;4364-80-1;tricyanovinylbenzene;NSC142326;SCHEMBL61242;DTXSID70301319;NSC-142326;A826667

Suppliers and Price of 2-Phenylethene-1,1,2-tricarbonitrile

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 7 raw suppliers

Chemical Property of 2-Phenylethene-1,1,2-tricarbonitrile

Chemical Property:

Vapor Pressure:0.00111mmHg at 25°C
Boiling Point:300.6°Cat760mmHg
Flash Point:137.1°C
Density:1.221g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:179.048347172
Heavy Atom Count:14
Complexity:366

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=C(C#N)C#N)C#N

Technology Process of 2-Phenylethene-1,1,2-tricarbonitrile

There total 5 articles about 2-Phenylethene-1,1,2-tricarbonitrile 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:

: 4364-80-1
2-phenyl-1,1,2-tricyanoethylene

Guidance literature:: With pyridine; diethyl ether;
DOI:10.1021/ja01544a057

Reference yield:

: 2700-22-3
Benzylidenemalononitrile

: 4364-80-1
2-phenyl-1,1,2-tricyanoethylene

Guidance literature:: Multi-step reaction with 2 steps

1: 2.57 g / ethanol; H₂O / 0.25 h / Heating

2: N-bromosuccinimide / CCl₄ / 8 h / Heating

With N-Bromosuccinimide; In tetrachloromethane; ethanol; water;