66252-12-8 Usage
Uses
Used in Pharmaceutical Industry:
2-Phenylnaphthalene-1-carbonitrile is used as an intermediate in the synthesis of various drugs, contributing to the development of new pharmaceuticals due to its unique chemical structure and properties.
Used in Dye and Pigment Production:
2-Phenylnaphthalene-1-carbonitrile is used as a precursor in the production of dyes and pigments, where its chemical composition plays a role in the color and stability of the final products.
Used in Liquid Crystal Manufacturing:
In the liquid crystal industry, 2-Phenylnaphthalene-1-carbonitrile is used as a component in the manufacturing process, leveraging its properties to influence the characteristics of liquid crystals for display and other applications.
Used in Organic Electronics and Optoelectronics:
2-Phenylnaphthalene-1-carbonitrile is used as a material in the field of organic electronics and optoelectronics, taking advantage of its electronic and optical properties to enhance the performance of devices in these sectors.
Overall, 2-Phenylnaphthalene-1-carbonitrile is a multifaceted compound with applications spanning across pharmaceuticals, dyes and pigments, liquid crystals, and organic electronics, highlighting its significance in the synthesis of a wide array of organic compounds and its contribution to various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 66252-12-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,5 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66252-12:
(7*6)+(6*6)+(5*2)+(4*5)+(3*2)+(2*1)+(1*2)=118
118 % 10 = 8
So 66252-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H11N/c18-12-17-15-9-5-4-8-14(15)10-11-16(17)13-6-2-1-3-7-13/h1-11H
66252-12-8Relevant academic research and scientific papers
Iron(II)-catalyzed direct cyanation of arenes with aryl(cyano)iodonium triflates
Shu, Zhibin,Ji, Wenzhi,Wang, Xi,Zhou, Yujing,Zhang, Yan,Wang, Jianbo
supporting information, p. 2186 - 2189 (2014/03/21)
A direct oxidative cyanation of arenes under FeII catalysis with 3,5-di(trifluoromethyl)phenyl(cyano)iodonium triflate (DFCT) as the cyanating agent has been developed. The reaction is applicable to wide range of aromatic substrates, including polycyclic structures and heteroaromatic compounds. Copyright
A microwave-assisted domino benzannulation reaction towards functionalized naphthalenes, quinolines, and isoquinolines
Wang, Yuqin,Tan, Cun,Zhang, Xiaofei,He, Qian,Xie, Yuyuan,Yang, Chunhao
, p. 6622 - 6629,8 (2012/12/12)
An efficient palladium/copper-catalyzed domino reaction was developed to yield functionalized naphthalenes, quinolines, and isoquinolines. The reactions of various substituted 1-phenylprop-2-yn-1-ols containing electron-donating (EDG) and electron-withdrawing (EWG) groups and 1-heteroarylprop-2-yn-1-ols worked well with this procedure. Both electron-rich and-deficient aryl halides were satisfactory substrates for this reaction. This domino benzannulation process involves a Sonogashira cross-coupling reaction, followed by isomerization to a chalcone, and finally an intramolecular condensation reaction.
