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Benzeneacetonitrile, α-(2-methylpropylidene)-, also known as 2-methyl-3-phenylpent-2-enenitrile, is an organic compound with the chemical formula C12H13N. It is a colorless to pale yellow liquid with a molecular weight of 173.24 g/mol. Benzeneacetonitrile, a-(2-methylpropylidene)- is characterized by its aromatic benzene ring, a nitrile group (-CN), and a 2-methylpropylidene bridge connecting the benzene ring to the acetonitrile moiety. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is essential to handle Benzeneacetonitrile, a-(2-methylpropylidene)- with care, following proper safety protocols to minimize potential health and environmental risks.

6519-10-4

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6519-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6519-10-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6519-10:
(6*6)+(5*5)+(4*1)+(3*9)+(2*1)+(1*0)=94
94 % 10 = 4
So 6519-10-4 is a valid CAS Registry Number.

6519-10-4Relevant academic research and scientific papers

Cascade Process for Direct Transformation of Aldehydes (RCHO) to Nitriles (RCN) Using Inorganic Reagents NH2OH/Na2CO3/SO2F2 in DMSO

Fang, Wan-Yin,Qin, Hua-Li

, p. 5803 - 5812 (2019/05/14)

A simple, mild, and practical process for direct conversion of aldehydes to nitriles was developed feathering a wide substrate scope and great functional group tolerability (52 examples, over 90% yield in most cases) using inorganic reagents (NH2OH/Na2CO3/SO2F2) in DMSO. This method allows for transformations of readily available, inexpensive, and abundant aldehydes to highly valuable nitriles in a pot, atom, and step-economical manner without transition metals. This protocol will serve as a robust tool for the installation of cyano-moieties to complicated molecules.

Stereoarrayed 2,3-Disubstituted 1-Indanols via Ruthenium(II)-Catalyzed Dynamic Kinetic Resolution-Asymmetric Transfer Hydrogenation

Cotman, Andrej Emanuel,Modec, Barbara,Mohar, Barbara

supporting information, p. 2921 - 2924 (2018/05/28)

Activated racemic 2,3-disubstituted 1-indanones 1 possessing two stereolabile centers were stereoselectively reduced to the corresponding chiral 2,3-disubstituted-1-indanols 2 by ruthenium(II)-catalyzed dynamic kinetic resolution-asymmetric transfer hydro

Direct synthesis of α,β-unsaturated nitriles in solid/liquid heterogeneous medium

Ladhar,El Gharbi

, p. 413 - 417 (2007/10/02)

α,β-unsaturated nitriles are obtained with high yields by condensation of diversely substituted aldehydes using nitriles in the presence of K2CO3. These basic active species avoids aldolisation generally observed in this type of reaction.

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