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197652-99-6

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197652-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197652-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,6,5 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 197652-99:
(8*1)+(7*9)+(6*7)+(5*6)+(4*5)+(3*2)+(2*9)+(1*9)=196
196 % 10 = 6
So 197652-99-6 is a valid CAS Registry Number.

197652-99-6Relevant academic research and scientific papers

1-(4-Alkyloxybenzyl)-3-methyl-1H-imidazol-3-ium organic backbone: A versatile smectogenic moiety

Dobbs, William,Douce, Laurent,Heinrich, Benoit

experimental part, (2010/04/22)

The merger of ionic liquid and liquid crystal fields, obtained by using the imidazolium ring as a common element, has allowed us to tailor a new set of materials which associate specific functionalities. These functionalities are consequences of the origi

Positional and charged effects of heterocyclic N atoms on mesogenic properties of stilbazoles and analogous N-oxides

Lin, Hong-Cheu,Lai, Long-Li,Lin, Yu-Sheng,Tsai, Chiitang,Chen, Rong-Chi

, p. 55 - 71 (2007/10/03)

The synthesis and the phase behavior of stilbazoles and corresponding N-oxides containing different positions of heterocyclic N atoms, i.e. trans-2′-, 3′-, 4′- stilbazoles and their N-oxides, are reported. Their phase transition temperatures and the mesog

Alkoxylated p-phenylenevinylene oligomers: Synthesis and spectroscopic and electrochemical properties

Ndayikengurukiye, Henri,Jacobs, Sven,Tachelet, Wim,Van Der Looy, Johan,Pollaris, Anne,Geise, Herman J.,Claeys, Magda,Kauffmann, Jean M.,Janietz, Silvia

, p. 13811 - 13828 (2007/10/03)

Twenty-one n-alkoxy substituted phenylenevinylene oligomers were synthesized, varying in size, number and position of the OR groups. IR,MS and solubility data are presented. NMR measurements provided the molecular structure as well as information about conformations and molecular dynamics. UV and of cyclic voltammetric data give correlations of chemical structure (number and position of OR substituents) with separate HOMO and LUMO energies.

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