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Tribenzylstibane is an organostibine compound with the chemical formula (C6H5CH2)3Sb. It is a derivative of stibine, where three benzyl groups (C6H5CH2-) are attached to the antimony atom. tribenzylstibane is characterized by its colorless, crystalline appearance and is relatively stable at room temperature. Tribenzylstibane is synthesized by reacting antimony trichloride with benzylmagnesium chloride, and it is used in various chemical reactions as a reagent or a precursor to other organostibine compounds. Due to its potential toxicity and environmental impact, handling and disposal of tribenzylstibane should be done with caution, following proper safety protocols.

5072-92-4

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5072-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5072-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,7 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5072-92:
(6*5)+(5*0)+(4*7)+(3*2)+(2*9)+(1*2)=84
84 % 10 = 4
So 5072-92-4 is a valid CAS Registry Number.

5072-92-4Relevant academic research and scientific papers

Vinyl and carbene ruthenium(II) complexes from hydridoruthenium(II) precursors

Jung, Stefan,Brandt, Carsten D.,Wolf, Justin,Werner, Helmut

, p. 375 - 383 (2007/10/03)

The reactions of the hydrido compounds [RuHCl(CO)(L)2] {L = PiPr3 (1), PCy3 (2)} with HC≡CR (R = H, Ph, tBu) afforded by insertion of the alkyne into the Ru-H bond the corresponding vinyl complexes [RuCl(CH=CHR)-(CO)(L)su

Selective formation of ethanol from methanol, hydrogen and carbon monoxide

-

, (2008/06/13)

A process for the selective formation of ethanol which comprises contacting methanol, hydrogen and carbon monoxide with a catalyst system comprising cobalt acetylacetonate, a tertiary organo Group V A compound of the periodic Table, a first promoter comprising an iodine compound and a second promoter comprising a ruthenium compound.

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