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(C6H2(CH3)3)2HGeGeH(C6H2(CH3)3)2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100418-05-1

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100418-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100418-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,1 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100418-05:
(8*1)+(7*0)+(6*0)+(5*4)+(4*1)+(3*8)+(2*0)+(1*5)=61
61 % 10 = 1
So 100418-05-1 is a valid CAS Registry Number.

100418-05-1Downstream Products

100418-05-1Relevant academic research and scientific papers

First characterization of a compound with a tin-germanium double bond: The dimesityl(diisitylstanna)germene (Is)2Sn=Ge(MeS)2

Chaubon, Marie-Anne,Escudie, Jean,Ranaivonjatovo, Henri,Satge, Jacques

, p. 2621 - 2622 (2007/10/03)

The dimesityl(diisitylstanna)germene 4 [isityl (Is) = 2,4,6-triisopropylphenyl] is synthesized by dehydrofluorination of the corresponding (fluorostannyl)germane 1 by tert-butyllithium at low temperature; its structure is evidenced at -20°C by 119Sn NMR spectroscopy (δ + 360), by addition of water and methanol to the tin-germanium double bond and by a [2 + 2] cycloaddition with benzaldehyde; warming the stannagermene 4 to room temperature affords the dimesityl(tetraisityldistanna)germirane 8.

Improved synthesis of 1,2-dichlorotetramesityldigermane and other mesitylgermanes

Cooke, Jeffrey A.,Dixon, Craig E.,Netherton, Matthew R.,Kollegger, Gerlinde M.,Baines, Kim M.

, p. 1205 - 1217 (2008/10/09)

An improved procedure for the synthesis of 1,2-dichlorotetramesityldigermane is reported.

Nouveaux aryldihydrogermyllithium

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

, p. 49 - 61 (2007/10/02)

The new aryldihydrogermyllithium complexes RH2GeLi (R = Ph, Mes) are prepared, in good yields, by metallation of the parent trihydrogermane with t-butyllithium in THF.They are characterized by alkylation reactions with MeI.Some germylation reactions are reported: they lead to the formation of new functional aryldihydrogermanes and aryldigermanes by a nucleophilic substitution.These aryldihydrogermyllithium complexes react also with acyl chlorides RCOCl (R = Ph, Mes) to give new diacyl- and triacyl-germanes.These easily add to the carbonyl group of aromatic aldehydes, thereby giving the corresponding α-germyl alcohols.

New (diarylgermyl)lithiums

Castel,Riviere,Satge,Ko

, p. 205 - 210 (2008/10/08)

The new (diarylgermyl)lithiums R2GeHLi (2; R = phenyl, mesityl) were prepared in good yields by hydrogermolysis reactions of tert-butyllithium in THF. The stability of compounds 2 depends on the nature of the R group and the solvent. For R = Ph, in the presence of an amine (Et3N or Et2NMe), the same reaction leads to the formation of the polygermanes H(GePh2)nH (n = 2-4). The characterization of compounds 2 by IR and 1H and 13C NMR spectroscopy and their complexation with a crown ether are also reported. They are characterized by deuterolysis and alkylation reaction (with MeI and Me2SO4). Their germylation reactions with Ge-Cl reagents constitute a convenient way for synthesizing organo-hydropolygermanes. Compounds 2 also react with acyl chlorides to give new germyl ketones, R2HGeCOR′, and the unexpectedly stable β-germyl diketone Ph2Ge(COMes)2.

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