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C6H5Ge(SCH3)3 is an organogermanium compound, consisting of a benzene ring (C6H5) bonded to a germanium atom, which in turn is connected to three methylthio (SCH3) groups. C6H5Ge(SCH3)3 is a derivative of triphenylgermane, with each hydrogen atom on the germanium atom replaced by a methylthio group. It is a colorless, crystalline solid that is sensitive to air and moisture. Due to the presence of the germanium atom and the thioether groups, C6H5Ge(SCH3)3 has unique chemical and physical properties that distinguish it from its carbon-based analogs. It is used in various chemical reactions and as a precursor in the synthesis of other organogermanium compounds.

3931-77-9

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3931-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3931-77-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,3 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3931-77:
(6*3)+(5*9)+(4*3)+(3*1)+(2*7)+(1*7)=99
99 % 10 = 9
So 3931-77-9 is a valid CAS Registry Number.

3931-77-9Downstream Products

3931-77-9Relevant 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.

ASSISTANCE NUCLEOPHILE DANS DES REACTIONS D'ORGANO-HALOGENO- ET -HALOGENO-HYDROGERMANES: GERMYLANIONS, GERMYLENES, DERIVES FONCTIONNELS DU GERMANIUM

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

, p. 123 - 136 (2007/10/02)

Substitution reactions of halogermanes under nucleophilic assistance of tertiary amines or diazo derivatives leading readily to various functional derivatives of germanium have been carried out.Dehydrohalogenation of acidic halohydrogemanes under nucleophilic assistance is a useful way to divalent species, and the germylenes formed are stabilized by complexation with the nucleophilic agent.The reactions proceed via intermediate halogermylanions which lead to the formation of more stable germylenes.The transient halogemylanions have been characterized by means of their nuclophilic additions to carbonyl derivatives.Nucleophilic substitutions of halogermanes using these germylanions lead to the formation of polygermanes.

SYNTHESE DE COMPOSES A LIAISON MIVB-MERCURE. PRECURSEURS D'ESPECES MONOVALENTES (GERMYNES), ET BIVALENTES (GERMYLENES), DE RADICAUX CENTROMETALLES ET D'INTERMEDIAIRES

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

, p. 351 - 367 (2007/10/02)

Polynuclear germyl-mercury compounds are obtained from the reaction of organohydrogermanes PhnGeH4-n or digermanes Ph2nGe2H4-n (n = 1, 2) with dialkylmercury R2Hg.Di- or tri-mercurated geminal polygermates thus synthesized generally present a low stability and undergo thermal- or photodecompositions leading to the corresponding monovalent (germynes), divalent (germylenes) or, trivalent (germanium centered radicals) species and also to intermediate biradicals which could be considered as limit forms of germanium doubly-bonded compounds .Such intermediates have been chemically and spectroscopically characterized.Extension of these reactions to the silicon analogs met with difficulties, and thus previously observed differences between silicon and germanium chemistry were confirmed.

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