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Tris(allyl)bismuth is an organobismuth compound with the chemical formula (C3H5)3Bi. It is a colorless, viscous liquid that is soluble in organic solvents. tris(allyl)bismuth is synthesized by reacting bismuth trichloride with allyl magnesium chloride. Tris(allyl)bismuth is of interest in organometallic chemistry due to its potential applications in various fields, such as catalysis and the synthesis of other organobismuth compounds. It is also known for its thermal stability and resistance to decomposition, which makes it a promising candidate for further research and development in the chemical industry.

94334-65-3

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94334-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94334-65-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,3 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94334-65:
(7*9)+(6*4)+(5*3)+(4*3)+(3*4)+(2*6)+(1*5)=143
143 % 10 = 3
So 94334-65-3 is a valid CAS Registry Number.

94334-65-3Downstream Products

94334-65-3Relevant academic research and scientific papers

The bis(allyl)bismuth cation: A reagent for direct allyl transfer by lewis acid activation and controlled radical polymerization

Lichtenberg, Crispin,Pan, Fangfang,Spaniol, Thomas P.,Englert, Ulli,Okuda, Jun

, p. 13011 - 13015 (2012)

Cationic organometallic compounds of Group 3 (including the lanthanoids), 4, or 13 elements show increased Lewis acidity and electrophilicity compared to their neutral parent compounds. They serve as efficient polymerization catalysts and as unique organometallic reagents for stoichiometric transformations.[1-3] The Lewis acidity of neutral bismuth(III) compounds has been recognized and exploited in bismuthcatalyzed (co)polymerizations and organic transformations.[4] However, the number of isolated and characterized cationic organobismuth(III) compounds is still limited, and detailed investigations concerning their reactivity have not been reported to date.[5, 6] Only two systems with chelating di(aryl) ligands have been applied as Lewis acid-base catalysts in organic transformations.[6] Herein, we present the isolation and characterization of the bis(allyl)bismuth cation and its application as an efficient allyl transfer reagent and as initiator for the controlled radical polymerization of styrene.

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