2,3,4,6-Tetramethylbenzonitrile

Base Information

Chemical Name:2,3,4,6-Tetramethylbenzonitrile
CAS No.:64648-35-7
Molecular Formula:C11H13N
Molecular Weight:159.231
Hs Code.:
DSSTox Substance ID:DTXSID50493105
Nikkaji Number:J3.411.113H
Wikidata:Q82339563

Synonyms:2,3,4,6-tetramethylbenzonitrile;64648-35-7;SCHEMBL8135367;DTXSID50493105;2,3,4,6-tetramethylphenyl cyanide

Suppliers and Price of 2,3,4,6-Tetramethylbenzonitrile

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 2,3,4,6-Tetramethylbenzonitrile

Chemical Property:

Melting Point:66-67 °C(Solv: ethanol (64-17-5))
Boiling Point:294.4±9.0 °C(Predicted)
PSA：23.79000
Density:0.96±0.1 g/cm3(Predicted)
LogP:2.79188
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:159.104799419
Heavy Atom Count:12
Complexity:200

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1C)C)C#N)C

Technology Process of 2,3,4,6-Tetramethylbenzonitrile

There total 4 articles about 2,3,4,6-Tetramethylbenzonitrile 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: 87.0%

: 4885-02-3
Dichloromethyl methyl ether

: 527-53-7
1,2,3,5-Tetramethylbenzene

: 64648-35-7
2,3,4,6-tetramethylbenzonitrile

Guidance literature:: Dichloromethyl methyl ether; 1,2,3,5-Tetramethylbenzene; With zinc dibromide; In dichloromethane; at 20 ℃; for 14h;

With ammonium hydroxide; iodine; In dichloromethane; at 20 ℃; for 6h;
DOI:10.1002/ejoc.201403672