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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)-

Iron, tricarbonyl[(1,2,3,4-h)-1,3,5,7-cyclooctatetraene]-

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Chemical Name: Iron, tricarbonyl[(1,2,3,4-h)-1,3,5,7-cyclooctatetraene]-
CAS Number: 12093-05-9
Product Number: AG003P5W(AGN-PC-0PFBMI)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
93-95℃ (lit.)
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
244.027g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
243.982g/mol
Monoisotopic Mass:
243.982g/mol
Topological Polar Surface Area:
51.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
88.4
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
4
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
5
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302+H312+H332
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tricarbonyl(cyclooctatetraene)iron(II) is a versatile organometallic compound that finds numerous applications in chemical synthesis. As a complex of iron with cyclooctatetraene ligands, this compound serves as a valuable source of iron in various reactions and processes. Its unique structure and reactivity make it a useful catalyst and reagent in the field of organic chemistry.In chemical synthesis, Tricarbonyl(cyclooctatetraene)iron(II) can act as a catalyst in a variety of transformations such as carbonylation reactions, cycloadditions, and metal-catalyzed coupling reactions. Its ability to facilitate carbon-carbon bond formation and functional group interconversions makes it a valuable tool for the efficient construction of complex organic molecules.Furthermore, Tricarbonyl(cyclooctatetraene)iron(II) can also mediate the selective reduction of carbonyl compounds to alcohols, making it a useful reagent for the synthesis of alcohol-containing compounds. Its relatively low toxicity and stable nature under standard laboratory conditions further contribute to its widespread use in organic synthesis.Overall, the unique properties and reactivity of Tricarbonyl(cyclooctatetraene)iron(II) make it an essential component in the toolkit of synthetic chemists, enabling the efficient and selective synthesis of various organic compounds.