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methyl-2,4,6-tribromophenylnitroxyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67384-84-3

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67384-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67384-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,8 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67384-84:
(7*6)+(6*7)+(5*3)+(4*8)+(3*4)+(2*8)+(1*4)=163
163 % 10 = 3
So 67384-84-3 is a valid CAS Registry Number.

67384-84-3Downstream Products

67384-84-3Relevant academic research and scientific papers

Oxiranylcarbinyl radicals from allyloxyl radical cyclization: Characterization and kinetic information via ESR spectroscopy

Grossi, Loris,Strazzari, Samantha,Gilbert, Bruce C.,Whitwood, Adrian C.

, p. 8366 - 8372 (1998)

An ESR spin-trapping technique has been used for the detection of oxiranylcarbinyl radicals as discrete reaction intermediates, formed via cyclization of allyloxyl radicals. The latter were obtained by photolysis of the corresponding nitrites, which were generated directly via an exchange reaction between the appropriate allylic alcohols and tert-butyl nitrite (which also acts as the spin-trap). Experiments have also been conducted with the spin-trap 2,4,6-tribromonitrosobenzene, which has allowed a study to be made of the competition between ring closure and β-scission of a variety of allyloxyl species.

Initiation of radical cyclisation reactions using dimanganese decacarbonyl. A flexible approach to preparing 5-membered rings

Gilbert, Bruce C.,Kalz, Wilhelm,Lindsay, Chris I.,McGrail, P. Terry,Parsons, Andrew F.,Whittaker, David T. E.

, p. 1187 - 1194 (2007/10/03)

Photolysis of dimanganese decacarbonyl [Mn2(CO)10] using visible light produces the manganese pentacarbonyl radical [Mn(CO)5] which reacts with organohalides to form carbon-centred radicals. Efficient halogen-atom abstract

FREE RADICALS. XXII. REACTIONS OF "ELECTRON-DEFICIENT" RADICALS WITH ORGANOMAGNESIUM AND ORGANOMERCURY COMPOUNDS

Tanaseichuk, B. S.,Belozerov, A. I.,Sanaeva, E. P.,Butin, K. P.

, p. 494 - 497 (2007/10/02)

The reactions of triphenylimidazolyl and diphenylaminyl radicals with methylmagnesium iodide, phenylmagnesium bromide, and dibenzylmercury were studied.It was shown that the radicals are reduced to anions and the radicals in the organometallic compounds are displaced.The homolytic nature of the displacement of the radical from the organometallic compounds ( SH2 reaction ) is confirmed by its capture by 2,4,6-tribromonitrosobenzene with formation of a nitroxyl radical.

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