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About This Item
Empirical Formula (Hill Notation):
C10H10Ru
CAS Number:
Molecular Weight:
231.26
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23
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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
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Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
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
M Wenzel et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 39(12), 1237-1241 (1988-01-01)
Ferrocene-Haloperidol was synthesized by N-alkylation of 4-(4'-chlorophenyl)- 4-hydroxypiperidine with 1-ferrocenyl-4-chlor-butan-1-on. By heating the ferrocene-haloperidol with 103RuCl3 the 103Ru-labelled ruthenocene-haloperidol was obtained. This compound showed a high affinity for lung but not for brain in rats and mice. The decay of
[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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