262455
Bis(cyclopentadienyl)ruthenium(II)
97%
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About This Item
Empirical Formula (Hill Notation):
C10H10Ru
CAS Number:
Molecular Weight:
231.26
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
EC Number:
215-065-2
MDL number:
InChI key
BKEJVRMLCVMJLG-UHFFFAOYSA-N
InChI
1S/2C5H5.Ru/c2*1-2-4-5-3-1;/h2*1-5H;
SMILES string
[Ru].[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2
assay
97%
form
solid
reaction suitability
core: ruthenium, reagent type: catalyst
mp
199-201 °C (lit.)
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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.
[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)
Adrenal-affinity of ruthenocenyl-derivatives of biogenic amines.
M Wenzel et al.
International journal of nuclear medicine and biology, 12(1), 1-2 (1985-01-01)
Annika Gross et al.
Bioconjugate chemistry, 23(9), 1764-1774 (2012-07-25)
Labeling of peptide nucleic acids (PNA) with metallocene complexes is explored herein for the modulation of the analytical characteristics, as well as biological properties of PNA. The synthesis of the first ruthenocene-PNA conjugate with a dodecamer, mixed-sequence PNA is described
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