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Bis(2,4-dinitrophenyl) diselenide, also known as 2,4-dinitrophenyldiselenide, is a chemical compound with the formula C12H6N4O8Se2. It is a yellow crystalline solid that is insoluble in water but soluble in organic solvents such as ethanol and acetone. bis(2,4-dinitrophenyl) diselenide is formed by the reaction of 2,4-dinitrophenol with selenium, resulting in a molecule that contains two 2,4-dinitrophenyl groups attached to a diselenium bridge. Bis(2,4-dinitrophenyl) diselenide is primarily used as a reagent in organic synthesis, particularly for the detection and determination of various functional groups in organic compounds. It is also known for its potential applications in the development of new materials and as a precursor in the synthesis of other organoselenium compounds. Due to its reactivity and potential toxicity, it is important to handle bis(2,4-dinitrophenyl) diselenide with care and in accordance with proper safety protocols.

1666-11-1

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1666-11-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1666-11-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1666-11:
(6*1)+(5*6)+(4*6)+(3*6)+(2*1)+(1*1)=81
81 % 10 = 1
So 1666-11-1 is a valid CAS Registry Number.

1666-11-1Relevant academic research and scientific papers

Synthesis of organic diselenide using zinc powder

Ping,Xunjun

, p. 1721 - 1725 (1993)

A new synthetic method of diselenide by reducing element selenium with zinc powder in basic environment, and then reacting with electrophiles is described. Nine diselenides are synthesized with yields between 52-90%.

LITHIUM DISELENIDE IN APROTIC MEDIUM - A CONVENIENT REAGENT FOR SYNTHESIS OF ORGANIC DISELENIDES

Syper, Ludwik,Mlochowski, Jacek

, p. 6119 - 6130 (2007/10/02)

The reduction of selenium with lithium in THF in the presence of diphenylacetylene as a catalyst afforded lithium diselenide, which reacted with electrophiles giving alkyl or aryl diselenides 1 - 3 and selenides 4, as by-products.The useful method for preparation of diselenides based on this reaction was elaborated.

Model Compounds for the Active Site Selenocysteine of Glutathione Peroxidase: a 77Se NMR Study

Dowd, Diane,Gettins, Peter

, p. 1 - 3 (2007/10/02)

To test the feasibility of using 77Se NMR to distinguish between different proposed mechanisms of action of the selenoenzyme glutathione peroxidase, model compounds containing the proposed selenium moieties have been synthesized and their 77Se NMR spectra recorded.It was found that the difference in chemical shift between the two proposed resting states, selenol or selenenic acid, is approximately 1300 ppm.For the next step, oxidation by hydrogen peroxide, a much smaller difference of about 100 ppm was found between selenenic and seleninic acid species.The products of the second reaction step, selenide sulfide vs selenoxide sulfide, differed in chemical shift by about 470 ppm.It was concluded that, for two of the three states of the enzyme, 77Se NMR could, in principle, be used unambiguously to distinguish between the two proposed mechanisms.KEY WORDS: 77Se NMR; glutathione peroxidase selenoenzyme; selenium model compounds.

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