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:
Quality Level
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
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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Results of ERBF and ERPF measurements in healthy dogs with two new radiopharmaceutical principles.
R de Jong et al.
Contributions to nephrology, 56, 49-52 (1987-01-01)
Malay Patra et al.
Chemical communications (Cambridge, England), 47(41), 11444-11446 (2011-09-22)
A convenient synthesis of azidomethyl-ruthenocene and its use in the covalent labelling of amino acids, peptides and a peptide nucleic acid (PNA) monomer derivative by Cu(I) catalyzed azide-alkyne coupling (Cu-AAC, "click chemistry") are described.
Cynthia T Sanderson et al.
Inorganic chemistry, 44(9), 3283-3289 (2005-04-26)
Electronic absorption and resonance Raman spectral studies of benzoylruthenocene (BRc) and 1,1'-dibenzoylruthenocene (DRc) indicate that the low-energy electronic excited states of these 4d(6) metallocenes possess metal-to-ligand charge transfer (MLCT) character. While this MLCT contribution should weaken the metal-ring bonding in
M Wenzel et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 37(6), 491-495 (1986-01-01)
The potential radiopharmaceuticals: ruthenocenoyl alanine, ruthenocenoyl methionine, 1'-methyl-ruthenocenoyl glycine and its esters were labelled with 103Ru starting from the analogous ferrocene compounds. In a series of tests in mice and rats these substances were compared with hippuran and ruppuran (=
M Wenzel et al.
Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al], 162(1), 51-56 (1986-01-01)
The organ distribution of 103Ru labelled ruthenocenyl derivatives of tyramine, histamine, benzylamine, phenylethylamine and homoveratrylamine were measured in rats. The derivatives of tyramine, histamine and benzylamine showed a high affinity for the adrenal and ovar. Adrenal/muscle ratios up to 2000:1
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