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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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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.
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
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
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
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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