4,4,4-Tribromobutanenitrile

Base Information

Chemical Name:4,4,4-Tribromobutanenitrile
CAS No.:62160-35-4
Molecular Formula:C4H4Br3N
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID80488281
Wikidata:Q82330848

Synonyms:4,4,4-Tribromobutanenitrile;tribromo-butyronitrile;62160-35-4;SCHEMBL11240058;DTXSID80488281

Suppliers and Price of 4,4,4-Tribromobutanenitrile

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 0 raw suppliers

Chemical Property of 4,4,4-Tribromobutanenitrile

Chemical Property:

Vapor Pressure:0.00211mmHg at 25°C
XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:304.78734
Heavy Atom Count:8
Complexity:106

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(CC(Br)(Br)Br)C#N

Technology Process of 4,4,4-Tribromobutanenitrile

There total 3 articles about 4,4,4-Tribromobutanenitrile 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:

: 75-25-2
Bromoform

: 107-13-1,25014-41-9
acrylonitrile

: 62160-35-4
γ-Tribrombutyronitril

Guidance literature:: With N-benzyl-trimethylammonium hydroxide; at 5 - 10 ℃; dann bei 25grad;
DOI:10.1021/ja01220a030

Reference yield:

: 75-25-2
Bromoform

: 920-34-3
2-bromoacrylonitrile

: 107-13-1,25014-41-9
acrylonitrile

: 62160-35-4
γ-Tribrombutyronitril

Guidance literature:: With sodium hydroxide; N-benzyl-N,N,N-triethylammonium chloride; In water; at 20 ℃; for 4h; Product distribution; When a mixture with α-bromoacrylonitrile was treated with a deficiency of bromoform under phase transfer conditions, only formation of 4,4,4-tribromo-butyronitrile was observed.;
DOI:10.1016/S0040-4039(01)84597-4