631507
1,10-Phenanthrolin-5-amine
97%
Sinonimo/i:
(1,10)-Phenanthrolin-5-ylamine
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1 G
171,00 €
5 G
540,00 €
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Cambia visualizzazione
1 G
171,00 €
5 G
540,00 €
About This Item
Formula empirica (notazione di Hill):
C12H9N3
Numero CAS:
Peso molecolare:
195.22
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
![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)
Livello qualitativo
Saggio
97%
Punto di fusione
254-258 °C (lit.)
Stringa SMILE
Nc1cc2cccnc2c3ncccc13
InChI
1S/C12H9N3/c13-10-7-8-3-1-5-14-11(8)12-9(10)4-2-6-15-12/h1-7H,13H2
DKPSSMOJHLISJI-UHFFFAOYSA-N
Categorie correlate
Applicazioni
1,10-Phenanthrolin-5-amine can be used in the synthesis of bis-[1,10]phenanthrolin-5-yl-pyromellitic diimide (Bphen-PMD), which can find applications in organic light-emitting devices.[1]
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Siew San Tan et al.
Physical chemistry chemical physics : PCCP, 19(37), 25734-25745 (2017-09-16)
An absorbance-based sensor employing ruthenium bipyridyl with a phenanthroline-fused benzoylthiourea moiety formulated as [Ru(ii)(bpy)
"Phenanthroline diimide as an organic electron-injecting material for organic light-emitting devices"
Lee H, et al.
Royal Society of Chemistry Advances, 2(23), 8762- 8767 (2012)
Mona Amiri et al.
Dalton transactions (Cambridge, England : 2003), 49(29), 10173-10184 (2020-07-16)
1,10-Phenanthroline (phen) was grafted to either indium tin oxide (ITO), fluorine-doped tin oxide (FTO), or titanium dioxide (TiO2) semiconductors (SC's) by electrochemical reduction of 5-diazo-phen. The phen ligand is bonded to the semiconductor at C5, and it can be handled
Barbara Feist et al.
Mikrochimica acta, 186(2), 91-91 (2019-01-12)
Graphene oxide (GO) was chemically functionalized with 5-amino-1,10-phenanthroline. The resulting conjugate (phen-GO) was characterized by scanning electron microscopy and X-ray photoelectron spectroscopy. The experiments show that phen-GO has a high affinity for extraction of Pb(II) ions. Isotherms and kinetics fit
Kollur Shiva Prasad et al.
Molecules (Basel, Switzerland), 25(12) (2020-06-26)
Herein we report the synthesis and structural elucidation of two novel imine-based ligands, 2-(1,10-phenanthrolin-5-yl)imino)methyl)-5-bromophenol (PIB) and N-(1,10-phenanthrolin-5-yl)-1-(thiophen-3-yl)methanimine (PTM) ligands. An in vitro cytotoxicity assay of the synthesized molecules was carried out against breast, cervical, colorectal, and prostate cancer cell lines
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