12203-31-5 Usage
Description
(Ethylbenzene)tricarbonylchromium(0) is a chemical compound that features a central chromium atom connected to three carbon monoxide ligands and an ethylbenzene molecule. (ETHYLBENZENE)TRICARBONYLCHROMIUM(0) is known for its strong reactivity, which is attributed to the chromium center and the electron-rich ethylbenzene ligand. It has been extensively studied for its potential applications in the synthesis of complex molecules and coordination chemistry, making it a significant compound for the development of new chemical processes and materials. Furthermore, it may also serve as a precursor for the synthesis of other organometallic compounds with potential industrial and pharmaceutical applications.
Uses
Used in Organic Chemistry:
(Ethylbenzene)tricarbonylchromium(0) is used as a catalyst for various reactions in organic chemistry, particularly for the formation of carbon-carbon and carbon-oxygen bonds. Its strong reactivity and unique structure make it a valuable tool in facilitating complex chemical transformations.
Used in Synthesis of Complex Molecules:
(ETHYLBENZENE)TRICARBONYLCHROMIUM(0) is utilized in the synthesis of complex molecules, where its reactivity and ability to form stable intermediates play a crucial role in constructing intricate molecular structures.
Used in Coordination Chemistry:
(Ethylbenzene)tricarbonylchromium(0) is employed in coordination chemistry for the study of its bonding and interactions with other molecules, which can lead to a better understanding of its properties and potential applications.
Used as a Precursor for Organometallic Compounds:
It may also be used as a precursor for the synthesis of other organometallic compounds, which can have potential applications in various industries, including pharmaceuticals and materials science.
Used in Industrial Applications:
(ETHYLBENZENE)TRICARBONYLCHROMIUM(0)'s unique properties and reactivity make it a promising candidate for the development of new industrial processes and materials, where its catalytic activity and ability to form stable intermediates can be harnessed for the production of valuable products.
Check Digit Verification of cas no
The CAS Registry Mumber 12203-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,2,2,0 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 12203-31:
(7*1)+(6*2)+(5*2)+(4*0)+(3*3)+(2*3)+(1*1)=45
45 % 10 = 5
So 12203-31-5 is a valid CAS Registry Number.
12203-31-5Relevant articles and documents
Rausch, M. D.,Moser, F. A.,Zaiko, E. J.,Lipman, A. L.
, p. 185 - 192 (1970)
Heterogeneous and homogeneous hydrogenation of styrene and stilbene chromium tricarbonyl complexes
Artemov,Sazonova,Lomakin
, p. 45 - 48 (2008/02/11)
Heterogeneous hydrogenation of the styrene and stilbene chromium tricarbonyl complexes by molecular hydrogen on skeletal nickel and palladium on carbon as catalysts was studied. As compared to styrene and stilbene, their arene chromium tricarbonyl analogs
Addition de Carbanions α Benchrotreniques sur Divers Aldehydes non Enolisables; Evolution des Produits Primaires d'Addition par Oxidation d'Oppenauer-Woodward, influence de la Substitution
Senechal-Tocquer, M. C.,Senechal, D.,Bihan, J. Y. Le,Gentric, D.,Caro, B.
, p. 353 - 364 (2007/10/02)
Aromatic hydrocarbons complexed with a Cr(CO)3 unit react with benzaldehydes and furfural in THF and in presence of t-BuOK at the benzylic position to give condensation products in good yields.Formation of ketones by in situ Oppenauer-Woodward oxidation is observed.Influence of ring substituents on this formation is discussed.
