934563-15-2 Usage
General Description
1,1-DIMETHYL-3,4-DIPHENYL-2-TRIMETHYLSILANYL-1H-SILOLE is a chemical compound with a unique structure that consists of a silicon atom bonded to a five-membered ring containing two methyl groups, two phenyl groups, and one trimethylsilyl group. 1,1-DIMETHYL-3,4-DIPHENYL-2-TRIMETHYLSILANYL-1H-SILOLE is classified as a silole, which is a type of organosilicon compound known for its potential applications in organic electronic devices and optoelectronics. Siloles have been studied for their luminescent properties and their ability to serve as electron-transporting materials in organic light-emitting diodes. These properties make 1,1-DIMETHYL-3,4-DIPHENYL-2-TRIMETHYLSILANYL-1H-SILOLE a promising candidate for the development of new materials in the field of advanced electronics and photonics.
Check Digit Verification of cas no
The CAS Registry Mumber 934563-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,4,5,6 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 934563-15:
(8*9)+(7*3)+(6*4)+(5*5)+(4*6)+(3*3)+(2*1)+(1*5)=182
182 % 10 = 2
So 934563-15-2 is a valid CAS Registry Number.
934563-15-2Relevant articles and documents
Formation of α-lithio siloles from silylated 1,4-dilithio-1,3- butadienes: Mechanism and applications
Luo, Qian,Wang, Chao,Gu, Li,Zhang, Wen-Xiong,Xi, Zhenfeng
experimental part, p. 1120 - 1128 (2011/07/09)
A full account of a useful transformation from silylated 1,4-dili-thio-1,3-butadienes to α-lithio siloles is described. These lithio siloles formed by this procedure are general, in terms of substitution patterns and synthetic methods, affording diversified silole derivatives. Notably, some structurally complex molecules, such as bridged bis-silole compounds, have been synthesized easily and successfully by applying our protocol. The structure of the α-lithio silole, which adopts a dimeric fashion through two lithium bridges, was confirmed by X-ray analysis. Furthermore, a possible mechanism of the skeleton rearrangements via E/Z isomerization of 1-silyl-1-lithio alkene and nucleophilic attack on silicon is proposed, and is also proved by experimental investigations. 2010 Wiley-VCH Verlag GmbH Co. KGaA, Weinheim.
