1,5-Hexadiene-1,1,6,6-tetracarbonitrile, 2,5-dimethyl-

Base Information

Chemical Name:1,5-Hexadiene-1,1,6,6-tetracarbonitrile, 2,5-dimethyl-
CAS No.:3695-97-4
Molecular Formula:C12H10N4
Molecular Weight:210.2346
Hs Code.:
DSSTox Substance ID:DTXSID70190447
Mol file:3695-97-4.mol

Synonyms:F 2394;BRN 2096565;1,5-HEXADIENE-1,1,6,6-TETRACARBONITRILE, 2,5-DIMETHYL-;1,1,6,6-Tetracyano-2,5-dimethyl-hexadien-(1,5);2,5-Dimethyl-1,5-hexadiene-1,1,6,6-tetracarbonitrile;3695-97-4;DTXSID70190447;LS-74909

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Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,5-Hexadiene-1,1,6,6-tetracarbonitrile, 2,5-dimethyl-

Chemical Property:

Vapor Pressure:1.12E-11mmHg at 25°C
Boiling Point:538.7°Cat760mmHg
Flash Point:278°C
Density:1.126g/cm³
XLogP3:2.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:210.090546336
Heavy Atom Count:16
Complexity:451

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 1,5-Hexadiene-1,1,6,6-tetracarbonitrile, 2,5-dimethyl-

There total 2 articles about 1,5-Hexadiene-1,1,6,6-tetracarbonitrile, 2,5-dimethyl- 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: 95.0%

: 110-13-4
2,5-hexanedione

: 109-77-3
malononitrile

: 3695-97-4
2,5-dimethylhexa-1,5-diene-1,1,6,6-tetracarbonitrile

Guidance literature:: With MIL-53(Fe) metal organic framework encapsulated on silica-coated nickel ferrite magnetic nanoparticles; In ethanol; at 20 ℃; for 2h;
DOI:10.1055/s-0037-1612076