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Tetrachloro-[1,4]benzoquinone, also known as 1,2,3,4-tetrachloro-p-benzoquinone, is a chemical compound with the formula C6Cl4O2. It is a yellow crystalline solid that is soluble in organic solvents. tetrachloro-[1,4]benzoquinone; compound with hexamethylbenzene is an important intermediate in the synthesis of various chemicals, including dyes and pharmaceuticals. When combined with hexamethylbenzene, a compound with the formula C12H18, the resulting mixture forms a complex that can be used in various chemical reactions and applications. Hexamethylbenzene is an aromatic compound with a symmetrical structure, consisting of a benzene ring with six methyl groups attached to each carbon atom. The combination of these two chemicals can lead to the formation of new compounds with unique properties, making them valuable in the field of organic chemistry and material science.

850-23-7

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850-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 850-23-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 0 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 850-23:
(5*8)+(4*5)+(3*0)+(2*2)+(1*3)=67
67 % 10 = 7
So 850-23-7 is a valid CAS Registry Number.

850-23-7Downstream Products

850-23-7Relevant academic research and scientific papers

Charge-transfer probes for molecular recognition via steric hindrance in donor-acceptor pairs

Rathore,Lindeman,Kochi

, p. 9393 - 9404 (1997)

Molecular association of various aromatic hydrocarbons (D, including sterically hindered donors) with a representative group of diverse acceptors (A = quinone, trinitrobenzene, tetracyanoethylene, tropylium, tetranitromethane, and nitrosonium) is visually apparent in solution by the spontaneous appearance of distinctive colors. Spectral (UV-vis) analyses of the colored solutions reveal their charge-transfer origin (λ(CT)) and they provide quantitative information of the intermolecular association in the form of the K(DA) and ε(CT) values for the formation and visualization, respectively, of different [D,A] complexes. Importantly, such measurements establish charge-transfer absorption to be a sensitive analytical tool for evaluating the steric inhibition of donor-acceptor association. For example, the steric differences among various hindered aromatic donors in their association with quinone are readily dramatized in their distinctive charge-transfer (color) absorptions and verified by X-ray crystallography of the charge-transfer crystals and/or QUANTA molecular modeling calculations of optimum intermolecular separations allowed by van der Waals contacts.

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