1,1-Dicyano-2-phenyl-2-(1-bromoethyl)ethylene

Base Information

Chemical Name:1,1-Dicyano-2-phenyl-2-(1-bromoethyl)ethylene
CAS No.:61404-69-1
Molecular Formula:C12H9BrN2
Molecular Weight:261.121
Hs Code.:
DSSTox Substance ID:DTXSID90393897

Synonyms:1,1-Dicyano-2-phenyl-2-(1-bromoethyl)ethylene;61404-69-1;SCHEMBL5744779;DTXSID90393897;AHRIITVCPAZZTJ-UHFFFAOYSA-N;2-bromo-1-phenyl-propylidene-propanedinitrile;2-(2-bromo-methyl-1-phenylethylidene)malononitrile

Suppliers and Price of 1,1-Dicyano-2-phenyl-2-(1-bromoethyl)ethylene

Supply Marketing:

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

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Chemical Property of 1,1-Dicyano-2-phenyl-2-(1-bromoethyl)ethylene

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:259.99491
Heavy Atom Count:15
Complexity:328

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 1,1-Dicyano-2-phenyl-2-(1-bromoethyl)ethylene

There total 3 articles about 1,1-Dicyano-2-phenyl-2-(1-bromoethyl)ethylene 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:

: C₁₂H₉N₂^(1-)*K⁽¹⁺⁾

: 61404-69-1
(2-Bromo-1-phenylpropylidene)propanedinitrile

Guidance literature:: With bromine; In tetrachloromethane; for 3h;
DOI:10.1039/b009175h

Reference yield:

: 93-55-0
1-phenyl-propan-1-one

: 109-77-3
malononitrile

: 61404-69-1
(2-Bromo-1-phenylpropylidene)propanedinitrile

Guidance literature:: With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; dibenzoyl peroxide; Yield given. Multistep reaction; 2.) carbon tetrachloride, UV light;