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Trimethylsilanylsulfanyl-trimethylsilanylsulfanylmethylsulfanyl-methane is a complex organosilicon compound with the molecular formula C6H18Si2S3. Trimethylsilanylsulfanyl-trimethylsilanylsulfanylmethylsulfanyl-methane is characterized by its unique structure, which includes two trimethylsilanyl groups (Si(CH3)3) and a central methane molecule (CH4), with each hydrogen atom on the methane molecule replaced by a sulfanyl group (-SH). The presence of these sulfanyl groups results in a highly reactive and versatile molecule, which can be used in various chemical reactions and applications, such as in the synthesis of other organosilicon compounds or as a reagent in organic synthesis. Due to its complex structure and potential reactivity, handling and storage of Trimethylsilanylsulfanyl-trimethylsilanylsulfanylmethylsulfanyl-methane require careful consideration of safety precautions and appropriate containment measures.

85090-31-9

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85090-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85090-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85090-31:
(7*8)+(6*5)+(5*0)+(4*9)+(3*0)+(2*3)+(1*1)=129
129 % 10 = 9
So 85090-31-9 is a valid CAS Registry Number.

85090-31-9Downstream Products

85090-31-9Relevant academic research and scientific papers

NEUE ERGEBNISSE BEI DER SPALTUNG VON THIOETHERN MIT NATRIUM IN FLUESSIGEM AMMONIAK. ABTRENNUNG VON 1.3.5-TRITHIAPENTAN UEBER 1.5-BIS-(TRIMETHYLSILYL)-1.3.5-TRITHIAPENTAN ALS ZWISCHENSTUFE

Weissflog, Eckhard

, p. 233 - 240 (2007/10/02)

Recent results show that the cleavage of oligomeric and polymeric thioformaldehydes or polymethylenedisulfide by sodium in liquid ammonia, followed by treatment with an excess of hydrochloric acid, leads to the formation of mercaptothioethers, CH3(SCH2)nSH, bis-mercaptothioethers, HS(CH2S)mH and thioalkanes, CH3(SCH2)xSCH3.The identification and isolation of various components of these mixtures are described.The separation of pure 1.3.5-trithiapentane by silylation, distillation and cleavage with hydrogen chloride is of interest for its synthesis starting from easily available compounds like s-trithiane, polymethylenesulfide or polymethylenedisulfide.The silylated derivatives of 1.3.5-trithiahexane and 1.3.5-trithiapentane are described.

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