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Merck

262455

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
NACRES:
NA.23
PubChem Substance ID:
24855742
UNSPSC Code:
12352103
EC Number:
215-065-2
MDL number:
MFCD00001442

Key Documents

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Product Name

Bis(cyclopentadienyl)ruthenium(II), 97%

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

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCX4488
MKCV3292
MKCQ7806
MKCP5799
MKCN2243

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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.
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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