2,2-Dimethylbutanenitrile

Base Information

Chemical Name:2,2-Dimethylbutanenitrile
CAS No.:20654-46-0
Molecular Formula:C6H11N
Molecular Weight:97.16
Hs Code.:
European Community (EC) Number:837-327-0
DSSTox Substance ID:DTXSID801318822
Nikkaji Number:J554.384C

Synonyms:2,2-dimethylbutanenitrile;20654-46-0;Dimethylaethylessigsaurenitril;DTXSID801318822;AKOS012320702;EN300-178260;Z1079179196

Suppliers and Price of 2,2-Dimethylbutanenitrile

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 3 raw suppliers

Chemical Property of 2,2-Dimethylbutanenitrile

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:97.089149355
Heavy Atom Count:7
Complexity:94

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2,2-Dimethylbutanenitrile

There total 1 articles about 2,2-Dimethylbutanenitrile 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:

: 926-04-5
3,3-dimethylbutanamide

: 20654-46-0
2,2-dimethylbutyronitrile

: 829-10-7
2,2-dimethyl-1-phenylbutanone

Guidance literature:: With diethyl ether; phenylmagnesium bromide; toluene;

Reference yield:

: 20654-46-0
2,2-dimethylbutyronitrile

: 595-37-9
2,2-dimethylbutyric acid

Guidance literature:: With hydrogenchloride; at 100 - 120 ℃;

Reference yield:

: 20654-46-0
2,2-dimethylbutyronitrile

: 136006-58-1
Sodium; (3R,5S)-6-{2-[(R)-cyclohexyl-(2,2-dimethyl-butyrylamino)-methyl]-4,6-dimethyl-phenoxy}-3,5-dihydroxy-hexanoate

Guidance literature:: Multi-step reaction with 3 steps

1: 490 mg / 48percent aq. HF / 50 h / 25 °C

2: 73 percent / glacial acetic acid, tetra-n-butylammonium fluoride trihydrate / tetrahydrofuran / 4 h / 20 °C

3: 1N NaOH / ethanol / 1 h / 20 - 25 °C

With sodium hydroxide; hydrogen fluoride; tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00114a004