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(C5H5)Fe(CO)2(CH2S(C6H5)2)(1+)*BF4(1-)=[(C5H5)Fe(CO)2(CH2S(C6H5)2)]BF4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97374-99-7

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97374-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97374-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,7 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 97374-99:
(7*9)+(6*7)+(5*3)+(4*7)+(3*4)+(2*9)+(1*9)=187
187 % 10 = 7
So 97374-99-7 is a valid CAS Registry Number.

97374-99-7Downstream Products

97374-99-7Relevant academic research and scientific papers

Kinetics and mechanism of cyclopropanation of cyclooctene by [Fe(η5-C5H5)(CO)2CH 2SPh2]BF4

McCarten, Paul,Barefield, E. Kent

, p. 4645 - 4648 (1998)

The kinetics of reaction of [Fe(η5-C5H5)(CO)2CH 2SPh2]BF4 with cyclooctene in CH2Cl2 solution have been studied under pseudo-first-order conditions at room temperature. The variation of kobs is nonlinear in both cyclooctene and added Ph2S. The results are interpreted in terms of a two-step reaction in which the cation [Fe(η5-C5H5)(CO)2CH 2SPh2]+ undergoes reversible, dissociative loss of Ph2S followed by competitive capture of the methyleneiron complex by cyclooctene to produce bicyclo[6.1.0]nonane. The methyleneiron intermediate is 4-5 times more reactive toward diphenylsulfide than cyclooctene. In the absence of added Ph2S, millimolar solutions of the iron complex react with cyclooctene at room temperature with a half-life of about 36 min to give >85% yields of bicyclo[6.1.0]nonane after 3 h, and it is thus more reactive than the dimethyl- and methylphenylsulfonium salt analogues.

Thallium(I)-promoted substitution reactions of chloromethyl complexes of iron and molybdenum with uncharged nucleophiles

Kent Barefield,McCarten, Paul,Hillhouse, M. Christine

, p. 1682 - 1684 (2008/10/08)

TIBF4 has been used as an electrophilic promotor for substitution of chloride in [Fe(η5-C5H5-(CO)2CH 2Cl] and [Mo(η5-C5H5)(CO)3CH 2Cl] by a wide range of uncharged nucleophiles. The resulting fluoroborate onium salts are obtained in high yield.

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