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Germane, bis(methylthio)diphenyl-, also known as bis(methylthio)diphenylgermane, is an organogermanium compound with the chemical formula C9H12GeS2. It is a colorless, crystalline solid that is sensitive to air and moisture. Germane, bis(methylthio)diphenyl- is formed by the combination of two methylthio groups (CH3S) with a diphenylgermane (C6H5)2Ge unit. Bis(methylthio)diphenylgermane is primarily used in the synthesis of various organogermanium compounds and as a precursor in the preparation of germanium-based materials for electronic and semiconductor applications. Due to its sensitivity to air and moisture, it is essential to handle Germane, bis(methylthio)diphenyl- under an inert atmosphere or in a glovebox to prevent degradation.

3860-83-1

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3860-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3860-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,6 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3860-83:
(6*3)+(5*8)+(4*6)+(3*0)+(2*8)+(1*3)=101
101 % 10 = 1
So 3860-83-1 is a valid CAS Registry Number.

3860-83-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(methylthio)diphenylgermane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3860-83-1 SDS

3860-83-1Downstream Products

3860-83-1Relevant academic research and scientific papers

Complexes du fer hydro-digermanies: 5-C5H5)(CO)2> (R = Et, Ph) - etude photolytique

Castel, A.,Riviere, P.,Ahbala, M.,Satge, J.,Soufiaoui, M.,Knouzi, N.

, p. 123 - 130 (2007/10/02)

The new complexes 5-C5H5)(CO)2> (R=Et or Ph) were prepared by a substitution reaction from the corresponding arylhalohydrodigermanes and the iron salt.Their characterization by IR, 1H and 13C NMR and mass spectroscopy is reported.Photolysis of each complex affords transient monohydrogermylcomplexes 5-C5H5)(CO)2> and dialkylgermylenes which are trapped by 3,5-di-tert-butylorthoquinone and dimethyldisulphide with correct yields.These photolytic reactions are not affected by radical initiators like peroxide.

REACTIONS DE DECHLORHYDRATATION D'ORGANOCHLOROHYDROGERMANES ET -POLYGERMANES

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

, p. C15 - C18 (2007/10/02)

1,8-Diazabicycloundec-7-ene appears to be an efficient dehydrochlorination agent for the organochlorohydrogermanes PhCl2GeH, R2ClGeH (R = Et, Ph).In diluted solutions the intramolecular α-elimination process leads to germylene through germanate

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 DE REDUCTION D'ORGANOHALOGENO- ET HALOGENO-GERMANES PAR DES REDUCTEURS DOUX R3M(IVB)-H ET RCHO: GERMYLANIONS, DERIVES FONCTIONNELS DU GERMANIUM

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

, p. 137 - 146 (2007/10/02)

Catalytic activity of nuclophiles such as tertiary amines and diazo derivatives in the reduction of halogermanes by means of gentle reductive agents, such as R3M(IVB)-H or RCHO, has been shown.In the particular case of enolisable aldehyde, a competition between nucleophilic substitution at the metal and germanium-halogen bond reduction has been observed.Transposition of enoxygermanes formed through the substitution process, leads to β-germylaldehydes.

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.

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