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2-(3-methylbut-2-en-1-yl)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118968-14-2

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118968-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118968-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,6 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118968-14:
(8*1)+(7*1)+(6*8)+(5*9)+(4*6)+(3*8)+(2*1)+(1*4)=162
162 % 10 = 2
So 118968-14-2 is a valid CAS Registry Number.

118968-14-2Relevant academic research and scientific papers

Photosubstitution of Dicyanobenzenes by Allylic Silanes, Germanes, and Stannanes via Photoinduced Electron Transfer

Nakanishi, Kazuhisa,Mizuno, Kazuhiko,Otsuji, Yoshio

, p. 2371 - 2379 (1993)

Photoreactions of 1,2- and 1,4-dicyanobenzenes (o- and p-DCB) with allylic silanes, germanes, and stannanes in acetonitrile were studied under various conditions.In these photoreactions, one of cyano groups of o- and p-DCB was replaced by allylic groups.W

A cascade approach to cyclic aminonitrones: reaction discovery, mechanism and scope

Sharma, Rojita,Bulger, Paul G.,McNevin, Michael,Dormer, Peter G.,Ball, Richard G.,Streckfuss, Eric,Cuff, James F.,Yin, Jingjun,Chen, G-Yi

supporting information; experimental part, p. 3194 - 3197 (2009/12/01)

Treatment of ω-epoxynitriles with hydroxylamine affords cyclic aminonitrones in a single step and with high stereoselectivity. The scope of this novel transformation was explored in a series of examples. The aminonitrone products were shown to be useful s

Asymmetric intramolecular arylcyanation of unactivated olefins via C-CN bond activation

Watson, Mary P.,Jacobsen, Eric N.

supporting information; experimental part, p. 12594 - 12595 (2009/04/10)

The enantioselective, intramolecular arylcyanation of unactivated olefins via C-CN bond activation has been accomplished using a Ni(0) catalyst and BPh3 co-catalyst. High enantioselectivities are achieved using TangPHOS as a chiral ligand. This method allows the generation of two new C-C bonds and one new quaternary carbon stereogenic center in a single synthetic step, converting readily available benzonitrile substrates into 1,1-disubstituted indanes in 49-85% yield and 92-97% ee. Copyright

PHOTOSUBSTITUTION OF DICYANOBENZENES BY GROUP 14 ORGANOMETALLIC COMPOUNDS VIA PHOTOINDUCED ELECTRON-TRANSFER. ADDITIVE AND MEDIUM EFFECTS ON PHOTOINDUCED ELECTRON TRANSFER REACTION

Mizuno, Kazuhiko,Nakanishi, Kazuhisa,Otsuji, Yoshio

, p. 1833 - 1836 (2007/10/02)

The phenanthrene-sensitized photoreaction of 1,2- and 1,4-dicyanobenzenes with group 14 organometallic compounds containing allylic and benzylic groups in CH3CN afforded the corresponding 1- and 4-allylated benzonitriles in high yields.These photoreactions were accelerated by the addition of Mg(ClO4)2 and benzene derivatives.

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