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1,3,5,2,4,6-Trioxatrigermin, 2,2,4,4,6,6-hexaethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67548-87-2

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67548-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67548-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,4 and 8 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67548-87:
(7*6)+(6*7)+(5*5)+(4*4)+(3*8)+(2*8)+(1*7)=172
172 % 10 = 2
So 67548-87-2 is a valid CAS Registry Number.

67548-87-2Downstream Products

67548-87-2Relevant academic research and scientific papers

POLYGERMANES PRECURSEURS D'ESPECES DU GERMANIUM A COORDINNANCE NON USUELLE

Riviere, P.,Castel, A.,Satge, J.,Guyot, D.

, p. 193 - 206 (2007/10/02)

Several thermal or photochemical α-elimination reactions of functional polygermanes lead to germylenes, R2Ge.Photolysis of polygermanes, cyclopolygermanes and polygermylmercury compounds and also hydrogen abstraction from various organohydropolygermanes using t-BuO., lead to the formation of polymetallated chains containing one or two germanium-centered radicals.These polygermyl radicals give germylenes, R2Ge, germanium centered radicals Ge., α-digermyl diradicals (or digermenes) Ge.-Ge. or Ge=Ge> and β- or γ-polygermyl diradicals via ahomolytic monoelectronic α-elimination process.In some cases the formation of α-digermyl diradicals or digermenes can also be seen as occuring through dimerization of germylenes but with lower yields.All these intermediates have been characterized by several trapping reactions with dimethyl disulfide, 2,3-dimethylbutadiene or biacetyl.

ADDITIONS DIPOLAIRES-1,3 EN SERIE GERMANIEE: ACTION DE NITRILIMINES, OXYDES DE NITRILE, ET NITRONES SUR LES GERMANONES ET GERMATHIONES

Lavayssiere, Helene,Satge, Jacques,Barrau, Jacques,Traore, Moussa

, p. 335 - 348 (2007/10/02)

A new aspect of the reactivity of germanone and germathiones towards nitrilimines, nitriloxides and nitrones is investigated.The regioselectivity of the dipolar 1,3-cycloaddition reactions between germanones or germathiones and diphenylnitrilimine is discussed.The structure of the adducts is determined from chemical or spectroscopic studies (13C NMR, IR).Germa-oxa- or -thia-diazolines, germaoxathiazoles and germaoxathiazolidines are obtained and the thermal stability of these adducts reported.

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