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4,7-Phenanthrolin
98%
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About This Item
Empirische Formel (Hill-System):
C12H8N2
CAS-Nummer:
Molekulargewicht:
180.21
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
98%
mp (Schmelzpunkt)
172-174 °C (lit.)
SMILES String
c1cnc2ccc3ncccc3c2c1
InChI
1S/C12H8N2/c1-3-9-10-4-2-8-14-12(10)6-5-11(9)13-7-1/h1-8H
InChIKey
DATYUTWESAKQQM-UHFFFAOYSA-N
Verwandte Kategorien
Allgemeine Beschreibung
4,7-Phenanthroline reacts with ruthenium carbonyl to yield cyclometalated derivatives.[1]
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Acute Tox. 4 Oral - Eye Dam. 1
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Javier A Cabeza et al.
Dalton transactions (Cambridge, England : 2003), 41(24), 7249-7257 (2012-05-10)
The reactions of [Ru(3)(CO)(12)] with four aromatic diazines have been studied in THF at reflux temperature. With phthalazine (L(1)), the compound [Ru(3)(μ-κ(2)N(2)N(3)-L(1))(μ-CO)(3)(CO)(7)] (1), which contains an intact phthalazine ligand in an axial position bridging an Ru-Ru edge through both N
H Olsen et al.
Environmental health perspectives, 102(5), 454-458 (1994-05-01)
This study examined the changes in cellular glucose uptake induced by 2,3,7,8 tetrachlorodibenzo-p-dioxin (TCDD) as measured by quantification of intracellular radioactivity in the NIH 3T3 L1 preadipocyte cell line after a 30-minute incubation with the non-metabolizable radioactive analogue of glucose
E Enan et al.
Reproductive toxicology (Elmsford, N.Y.), 10(3), 191-198 (1996-05-01)
This study examined the changes in cellular glucose uptake, cAMP-dependent protein kinase (PKA), and progesterone production induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in human luteinizing granulosa cells (LGCs) in culture. The role of Ah receptor on TCDD-mediated toxicity in human LGCs was
Miguel A Galindo et al.
Journal of inorganic biochemistry, 102(5-6), 1025-1032 (2008-01-12)
The reaction between [(eta(6)-p-cymene)Ru(H2O)3]X2 and 4,7-phenanthroline (phen) leads to the formation of the rectangular tetranuclear complexes [(eta(6)-p-cymene)4Ru4(mu-4,7-phen-N4,N7)(2)(mu-OH)4]X4 (X=NO3, 1a; SO3CF3, 1b) which have been structurally characterised by X-ray crystallography. 1H NMR spectroscopic studies suggest the presence of a partially dissociated
V Arluison et al.
Biochemistry, 37(20), 7268-7276 (1998-06-04)
RNA:pseudouridine synthetase (Pus1) from Saccharomyces cerevisiae is a multisite specific enzyme that catalyzes the formation of pseudouridine at positions 34 and 36 of intron-containing precursor tRNAIle and at positions 27 and/or 28 of several yeast tRNAs. In this paper we
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