66252-12-8 Usage
General Description
2-Phenylnaphthalene-1-carbonitrile is a chemical compound with the molecular formula C18H13N. It is a crystalline solid with a pale yellow to white color and is insoluble in water. 2-Phenylnaphthalene-1-carbonitrile is used in research and as a building block for the synthesis of other organic compounds. It has applications in the pharmaceutical industry for the production of various drugs, as well as in the production of dyes and pigments. It is also used in the manufacturing of liquid crystals and other organic materials. Additionally, 2-Phenylnaphthalene-1-carbonitrile has potential applications in the field of organic electronics and optoelectronics due to its unique electronic and optical properties. Overall, this compound has a range of industrial and research-based applications and is important in the synthesis of various organic compounds.
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 articles and documents
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
Phthalazines. XV. Ring transformation of phthalazines into naphthalenes by means of inverse-electron-demand Diels-Alder reaction
Oishi,Taido,Iwamoto,Miyashita,Higashino
, p. 3268 - 3272 (2007/10/02)
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