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Sigma-Aldrich

Bis(cyclopentadienyl)ruthenium(II)

97%

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About This Item

Empirical Formula (Hill Notation):
C10H10Ru
CAS Number:
1287-13-4
Molecular Weight:
231.26
EC Number:
215-065-2
MDL number:
MFCD00001442
UNSPSC Code:
12352103
PubChem Substance ID:
24855742
NACRES:
NA.23

Assay

97%

form

solid

reaction suitability

core: ruthenium
reagent type: catalyst

mp

199-201 °C (lit.)

SMILES string

[Ru].[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2

InChI

1S/2C5H5.Ru/c2*1-2-4-5-3-1;/h2*1-5H;

InChI key

BKEJVRMLCVMJLG-UHFFFAOYSA-N

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Description
Pricing

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Karin Schlotter et al.
Journal of medicinal chemistry, 48(11), 3696-3699 (2005-05-27)
Metallocene-derived bioisosteres lead to exceptionally strong binding G-protein-coupled receptor ligands, indicating substantial plasticity of the receptor excluded volume. Novel binding profiles of ferrocenylcarboxamides combining subnanomolar Ki values for the dopamine D4 receptor (1a, 0.52 nM; 1b, 0.63 nM) with superpotent
M Wenzl et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 39(10), 1023-1027 (1988-01-01)
Ruthenocene amphetamine analogues have the same brain uptake as iodo-labelled amphetamines. This paper compares the organ-distribution of 103Ru labelled ruthenocene- or ferrocene-amphetamine analogues in mice and rats with the same amphetamine in which H-atoms were partly substituted by D-atoms. The
Annika Gross et al.
Dalton transactions (Cambridge, England : 2003), 40(6), 1382-1386 (2010-12-25)
Organometallic conjugates of receptor-targeting peptides are proposed as interesting candidates for novel cancer therapies since they are capable of targeting a specific kind of cell. Here, we have synthesised a dicobalt hexacarbonyl alkyne compound linked to the neurotensin peptide hormone.
Damian Plażuk et al.
Organic & biomolecular chemistry, 9(2), 408-417 (2010-10-23)
(D)-Biotin was used for Friedel-Crafts acylation of electron-rich aromatic molecules--ferrocene, ruthenocene and pyrene. The reaction carried out in the presence of trifluoroacetic anhydride and trifluoromethanesulfonic acid afforded the corresponding biotinylarenes in moderate yields. These compounds, although lacking an amide bond
[Metabolism of 103 Ru-ruthenocene--in vitro experiments and a possible in vivo test for hydroxylases].
M Wenzel et al.
The International journal of applied radiation and isotopes, 32(11), 797-802 (1981-11-01)
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