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Benzaldehyde, 4-[(2-ethylhexyl)oxy]-2,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

182355-16-4

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182355-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 182355-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,3,5 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 182355-16:
(8*1)+(7*8)+(6*2)+(5*3)+(4*5)+(3*5)+(2*1)+(1*6)=134
134 % 10 = 4
So 182355-16-4 is a valid CAS Registry Number.

182355-16-4Relevant academic research and scientific papers

Synthesis and nonlinear optical properties of chromophores for photorefractive polymer materials

Font-Sanchis, Enrique,Céspedes-Guirao, Francisco J.,Sastre-Santos, ángela,Villacampa, Belén,Orduna, Jesús,Alicante, Raquel,Fernández-Lázaro, Fernando

experimental part, p. 4513 - 4520 (2009/10/02)

The synthesis and nonlinear optical (NLO) properties of a series of nitrostilbene-, dinitrostilbene-, and dicyanomethylenedihydrofuran-based chromophores potentially useful in photorefractive multifunctional polymers are reported. Electronic absorption sp

The synthesis of an electronically asymmetric substituted poly(arylenevinylene); poly{2-(2′-ethylhexyloxy)-5-[(E)-4″-nitrostyryl]-1,4- phenylenevinylene}

Gordon, John,Sheldon, Timothy J.,Bradley, Donal D. C.,Burn, Paul L.

, p. 1253 - 1258 (2007/10/03)

We have found that by the inclusion of a conjugated spacer it is possible to synthesise a poly(1,4-phenylenevinylene) derivative with an electron-withdrawing group attached directly from the substituted monomer. We describe a route for the synthesis of an electronically asymmetric styryl-derivatised poly(1,4-phenylenevinylene). The preparation was achieved in two steps from the nitrostyryl-substituted arylenedimethylene bisbromo monomer 13. In the first step, base-induced polymerisation of 13 afforded the soluble and processible precursor polymer 14. The precursor polymer 14 could then be converted in the second step to the insoluble and unprocessible conjugated polymer 15 by thermal treatment in the solid state.

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