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1-chlorodimethylstannyl-2-methyl(phenyl)borylferrocene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

223114-84-9

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223114-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 223114-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,1,1 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 223114-84:
(8*2)+(7*2)+(6*3)+(5*1)+(4*1)+(3*4)+(2*8)+(1*4)=89
89 % 10 = 9
So 223114-84-9 is a valid CAS Registry Number.

223114-84-9Relevant academic research and scientific papers

Fluoride-promoted aryl and allyl migration from boron to tin in 1-stannyl-2-borylferrocenes

Boshra, Ramez,Doshi, Ami,Jaekle, Frieder

, p. 1534 - 1541 (2009/01/31)

Transmetalation reactions where organotin reagents are used for the transfer of organic groups to boron halides are among the most selective and hence synthetically useful methods for the preparation of organoboranes. We describe here a rare example of the reverse reaction, where migration of the organic group from boron to tin is promoted by addition of fluoride. The bidentate Lewis acids Fc(BMeR)(SnMe2Cl) (Fc = 1,2-ferrocenediyl; R = phenyl (Ph), thienyl (Th), allyl (All)) react with KF at 45°C to give the rearranged fluoroboranes Fc(BMeF)(SnMe2R) as oily liquids. With an excess of KF, the fluoroborate complexes K[Fc(BMeF2)(SnMe 2R)] are obtained, which are readily isolated as light yellow solids in good to high yields. For the phenyl derivative it was demonstrated that the borate salt can be converted back to the fluoroborane by treatment with Me 3SiOTf or addition of pyridine, which gives the adduct Fc(BMeF)(SnMe2Ph) · Py as a crystalline solid. The fluoride and pyridine complexes have been characterized by multinuclear NMR spectroscopy, elemental analysis, and single-crystal X-ray diffraction (for R = Ph). Preliminary mechanistic studies suggest an intramolecular process and indicate that Lewis acid induced Sn-F bond activation may play an important role.

Ferrocene-based heteronuclear bidentate Lewis acids via highly selective ortho-borylation of 1,1′-bis(trimethylstannyl)ferrocene

Gamboa, Juan A.,Sundararaman, Anand,Kakalis, Lazaros,Lough, Alan J.,J?kle, Frieder

, p. 4169 - 4181 (2008/10/08)

The borylation of 1,1′-bis(tri-methylstannyl)ferrocene for the preparation of disubstituted ferrocenes was investigated. The reaction provided the route for the formation of a kind of ferrocene-based heteronuclear bidentate Lewis acids. Steric and electronic factors controlled the rate of the reaction. Nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry and elemental analysis were used to characterize the heteronuclear bidentate Lewis acids.

Selective synthesis of 1-stanna-2-boraferrocenes: novel bidentate Lewis acids via an unexpected rearrangement reaction

Jaekle, Frieder,Lough, Alan J.,Manners, Ian

, p. 453 - 454 (2007/10/03)

Ferrocene based bidentate Lewis acids of the general formula 1,2-fc(BR2)(SnR3) are obtained in one step from 1,1'-distannaferrocenes and chloroboranes via an unexpected rearrangement reaction.

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