Vanadium, dichlorobis(h5-2,4-cyclopentadien-1-yl)-


Chemical Name: Vanadium, dichlorobis(h5-2,4-cyclopentadien-1-yl)-
CAS Number: 12083-48-6
Product Number: AG003OAE(AGN-PC-0PF826)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties


Properties
MP:
182-194℃ (dec.)(lit.)
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid

Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
3285
Hazard Statements:
H301-H315-H319-H335
Precautionary Statements:
P261-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



Bis(cyclopentadienyl)vanadium dichloride, also known as V(Cp)2Cl2, is a versatile organometallic compound frequently utilized in chemical synthesis. This compound plays a crucial role in various organic transformations due to its ability to act as a catalyst or reagent in several reactions.In chemical synthesis, Bis(cyclopentadienyl)vanadium dichloride is commonly employed as a catalyst for olefin polymerization reactions, such as the polymerization of ethylene and propylene. Its unique structure and reactivity enable it to facilitate the formation of high molecular weight polymers with desirable properties.Furthermore, V(Cp)2Cl2 is often utilized in cycloaddition reactions, specifically in the synthesis of heterocycles and complex organic molecules. Its ability to participate in cycloaddition reactions provides a valuable tool for the construction of diverse chemical structures with high efficiency.Moreover, Bis(cyclopentadienyl)vanadium dichloride can also serve as a reagent in organic transformations, including C-C bond formation and functional group interconversions. Its versatility and reactivity make it a valuable resource for synthetic chemists seeking to access novel compounds and complex molecular architectures.Overall, the application of Bis(cyclopentadienyl)vanadium dichloride in chemical synthesis highlights its importance as a catalyst and reagent for a wide range of organic transformations, making it a valuable tool in modern synthetic chemistry.