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37,38,39,40,41,42-hexabutoxycalix<6>arene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

123240-83-5

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123240-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123240-83-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,4 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 123240-83:
(8*1)+(7*2)+(6*3)+(5*2)+(4*4)+(3*0)+(2*8)+(1*3)=85
85 % 10 = 5
So 123240-83-5 is a valid CAS Registry Number.

123240-83-5Downstream Products

123240-83-5Relevant academic research and scientific papers

Tailoring the selectivity and stability of chemically modified platinum nanocatalysts to design highly durable anodes for PEM fuel cells

Genorio, Bostjan,Subbaraman, Ram,Strmcnik, Dusan,Tripkovic, Dusan,Stamenkovic, Vojislav R.,Markovic, Nenad M.

supporting information; scheme or table, p. 5468 - 5472 (2011/07/08)

Big and small: Chemically modifying platinum with calix[4]arene yields a highly stable anode catalyst that effectively suppresses the oxidation reduction reaction without altering the maximum activity for the hydrogen oxidation reaction (see picture, Ptblue, Cgray, Ored, Syellow). This behavior extends from long-range-ordered stepped single-crystal surfaces to nanocatalysts. Copyright

Perforated Monolayers: Design and Synthesis of Porous and Cohesive Monolayers from Mercurated Calixarenes1

Markowitz, Michael A.,Janout, Vaclav,Castner, David G.,Regen, Steven L.

, p. 8192 - 8200 (2007/10/02)

Mercuration of a series of O-alkylated calixarenes (produced via reaction of tetrahydroxycalixarene, pentahydroxycalixarene hexahydroxycalixarene, and heptahydroxycalixarene with n-bromobutane and with n-bromohexadecane) affords an homologous series of calixarene-based surfactants that form stable monolayers at the air-water interface.Surface pressure-area isotherms, measured for each calixarene, yield limiting areas that are in excellent agreement with values predicted from space-filling models, if it is assumed that the base of each calixarene is parallel and the alkyl chains are perpendicular to the water surface.Introduction of malonic acid to the aqueous subphase results in a substantial increase in the coheresiveness of films derived from calixarene-, calixarene-, and calixarene-based surfactants, as judged by changes in surface viscosity.X-ray photoelectron spectroscopic analysis of a Langmuir-Blodgett film, produced from a malonic acid stabilized calixarene monolayer, shows a carboxylate/mercury ratio of 0.9.This value is in excellent agreement with a model that assumes that all of the bound malonate acts as a bridge between adjacent calixarene subunits in an hexagonally packed array.Water evaporation studies, carried out at the air-water interface, reveal that each of the calixarene-, calixarene-, and calixarene-based monolayers, in the presence and in the absence of malonic acid, maintains a porous structure that offers little resistance to the permeation of water, relative to a densely packed aliphatic monolayer of surfactant.

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