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η5-Cyclopentadienylbis(carbonyl)(1-phenylthiopropyl)iron(II) is a complex organometallic compound with the chemical formula C18H15FeO2S. It features a central iron(II) atom coordinated to a cyclopentadienyl ligand, two carbonyl groups, and a 1-phenylthiopropyl ligand. The cyclopentadienyl ligand is a five-membered ring with a η5 bonding mode, meaning it donates five electrons to the iron center. The two carbonyl groups (CO) are linear two-electron donor ligands, while the 1-phenylthiopropyl ligand is a three-carbon chain with a phenyl group and a sulfur atom attached to one end. η5-cyclopentadienylbis(carbonyl)(1-phenylthiopropyl)iron(II) is of interest in organometallic chemistry and may have potential applications in catalysis and materials science.

97970-08-6

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97970-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97970-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97970-08:
(7*9)+(6*7)+(5*9)+(4*7)+(3*0)+(2*0)+(1*8)=186
186 % 10 = 6
So 97970-08-6 is a valid CAS Registry Number.

97970-08-6Downstream Products

97970-08-6Relevant academic research and scientific papers

DIRECT CONVERSION OF ALKENES INTO METHYL-SUBSTITUTED CYCLOPROPANES USING AN ORGANOIRON ETHYLIDENE TRANSFER REAGENT

Kremer, Kenneth A. M.,Helquist, Paul

, p. 231 - 252 (2007/10/02)

(η5-C5H5)(CO)2FeCH(CH3)SPh (8) serves as a quite useful reagent for the transfer of ethylidene groups to alkenes to give methyl-substituted cyclopropanes in good yields.The reaction is accomplished by allowing 8 to react with an alkylating agent such as trimethyloxonium tetrafluoroborate or methyl fluorosulfonate in the presence of the alkene substrate.The active ethylidene transfer reagent is apparently a sulfonium salt which is too reactive to be isolated under normal conditions.In all csases, cyclopropanes are obtained stereospecifically with respect to the configuration of the starting alkenes, and with certain classes of substrates such as cis-disubstituted alkenes, the reaction also occurs with very high syn-stereoselectivity.

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