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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Ferrocene, ethenyl-

[CH-]1C=CC=C1.C=C[C-]1C=CC=C1.[Fe+2] Request for Quotation
Chemical Name: Ferrocene, ethenyl-
CAS Number: 1271-51-8
Product Number: AG000WO6(AGN-PC-0PIGNH)
Synonyms:
MDL No:
Molecular Formula: C12H12Fe
Molecular Weight: 212.0687

Identification/Properties

Properties
MP:
51-53 °C(lit.)
BP:
80-85 °C0.2 mm Hg(lit.)
Storage:
Keep in dry area;2-8℃;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
1325
Hazard Statements:
H228
Precautionary Statements:
P210
Class:
4.1
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


Vinylferrocene is a versatile organometallic compound that finds widespread application in chemical synthesis. One of its key uses is as a precursor for the synthesis of various functional materials and polymers through polymerization reactions. Vinylferrocene can undergo different types of polymerization processes, including radical polymerization and ring-opening metathesis polymerization, to yield polymers with tailored properties.In addition to its role in polymer synthesis, vinylferrocene is employed in the preparation of organometallic complexes and catalysts. It can serve as a ligand in transition metal catalyzed reactions, enhancing the reactivity and selectivity of the catalyst system. The presence of the ferrocene moiety in such complexes imparts unique redox properties, making them valuable in a variety of organic transformations.Furthermore, vinylferrocene is utilized in the construction of molecular switches and sensors due to its ability to undergo reversible redox processes. By incorporating vinylferrocene units into the design of these molecular systems, researchers can achieve stimuli-responsive materials that exhibit controlled switching behavior in response to external stimuli such as light or pH changes.Overall, the diverse applications of vinylferrocene in chemical synthesis highlight its significance in the development of novel materials, catalysts, and functional molecules with tailored properties and functionalities.