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About This Item
Empirical Formula (Hill Notation):
C12H8N2
CAS Number:
Molecular Weight:
180.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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![Pyrazino[2,3-f][1,10]phenanthroline 99% (HPLC)](/deepweb/assets/sigmaaldrich/product/structures/226/341/31d3909e-6700-4a3e-bfb3-9ed1f6b66ee2/640/31d3909e-6700-4a3e-bfb3-9ed1f6b66ee2.png)
Assay
98%
mp
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
InChI key
DATYUTWESAKQQM-UHFFFAOYSA-N
General description
4,7-Phenanthroline reacts with ruthenium carbonyl to yield cyclometalated derivatives.
Application
4,7-Phenanthroline was used in preparation of:
- cyclic tetranuclear half-sandwich ruthenium(II) complexes
- positively charged homochiral cyclic trinuclear metallacalix[3]arene species
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1
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
Certificates of Analysis (COA)
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Miguel A Galindo et al.
Dalton transactions (Cambridge, England : 2003), (10)(10), 1563-1566 (2004-07-15)
Reaction of [(dach)Pd(NO3)2] entities (dach = (R,R)-1,2-diaminocyclohexane, (S,S)-1,2-diaminocyclohexane) and 4,7-phenanthroline (phen) providing, respectively, 90 and 120 degrees bond angles, leads to the formation of two novel positively charged homochiral cyclic trinuclear metallacalix[3]arene species [((R,R)-1,2-diaminocyclohexane)Pd(phen)]3(NO3)6 (2a) and [((S,S)-1,2-diaminocyclohexane)Pd(phen)]3(NO3)6 (2b). These species
H Ashida et al.
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The effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on lipid peroxidation, 3H-Me-glucose (3H-Me-glu), and 14C-dehydroascorbic acid (14C-DHA) uptakes were studied in adipose tissue of male guinea pig. Under in vitro test conditions, using isolated adipose tissue in a culture medium (explant culture), TCDD
Bennett J D Datu et al.
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The exit from dauer in the free-living nematode Caenorhabditis elegans is under the control of a single amphidial neuron (ASJ) of the insulin-like signalling pathway. Mutations of this pathway have the ability to suppress entry into the dauer stage. It
Tina P Andrejević et al.
Journal of inorganic biochemistry, 208, 111089-111089 (2020-05-23)
Three novel Zn(II) complexes, [ZnCl2(qz)2] (1), [ZnCl2(1,5-naph)]n (2) and [ZnCl2(4,7-phen)2] (3), where qz is quinazoline, 1,5-naph is 1,5-naphthyridine and 4,7-phen is 4,7-phenanthroline, were synthesized by the reactions of ZnCl2 and the corresponding N-heterocyclic ligand in 1:2 molar ratio in ethanol at
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
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