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nonamethylphenylcyclopentasilan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57171-36-5

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57171-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57171-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,7 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57171-36:
(7*5)+(6*7)+(5*1)+(4*7)+(3*1)+(2*3)+(1*6)=125
125 % 10 = 5
So 57171-36-5 is a valid CAS Registry Number.

57171-36-5Downstream Products

57171-36-5Relevant academic research and scientific papers

Cyclopentasilanderivate mit Uebergangselementen

Hengge, E.,Siegl, H.,Stadelmann, B.

, p. 187 - 192 (1994)

By use of salt elimination, the transition-metal-substituted cyclopentasilanes Me9Si5-Co(CO)3PPh3, Me9Si5-Fe(CO)2Cp, Me9Si5-SiMe2Co(CO)3PPh3 and Me9Si5-SiMe2Fe(CO)2Cp were prepared and characterized.Key words: Silicon; Phosphorus; Iron; Cobalt; Silane; Mo

PROPERTIES AND REACTIONS OF OCTADECAMETHYLBICYCLODECYSILANE

Jenkner, Peter K.,Hengge, Edwin

, p. 25 - 32 (2007/10/02)

The title compound was synthesized by a Wurtz-type condensation of dichlorotetramethyldisilane and trichloromethylsilane under selected conditions.Isolation from a mixture of several other permethylated cyclic, catenated and cage oligosilanes was achieved by RP-HPLC and RP-MPLC methods.ESR-investigations upon chemical reduction were carried out at different temperatures.Reactivity is shown to be distincly different to that of medium-sized monocyclic permethyloligosilanes.The isomeric bi(nonamethylcyclopentasilanyl) was also prepared and pathways to other oligocyclic methylsilanes are shown, starting from monofunctional cyclopentasilanes.

SYNTHESIS AND PROPERTIES OF SUBSTITUTED METHYLCYCLOPOLYSILANES

Helmer, Bradley J.,West, Robert

, p. 21 - 32 (2007/10/02)

Co-condensation of five equivalents Me2SiCl2 and one equivalent RR'SiCl2 with lithium provides the five- and six-membered rings RR'Si(Me2Si)4 and RR'Si(Me2Si)5.This method provides a direct route to the phenyl substituted methylcyclopolysilanes (R,R'=Me, Ph) which can be used for further functionalization of the silicon rings.It also provides several new sterically hindered methylcyclopolysilanes (R,R'=Ph, Ph; Me, t-Bu) which could not be synthesized by the conventional demethylation routes.These products have all been isolated and characterized by their ultraviolet, 1H-, 13C- and 29Si-NMR spectra.

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