4,7-Dimethyl-1,10-phenanthroline, 98%
4,7-Dimethyl-1,10-phenanthroline, 98%
4,7-Dimethyl-1,10-phenanthroline, 98%
Thermo Scientific Chemicals

4,7-Dimethyl-1,10-phenanthroline, 98%

CAS: 3248-05-3 | C14H12N2 | 208.26 g/mol
数量:
0.25 g
1 g
5 g
製品番号(カタログ番号) A17779.03
または、製品番号A17779-03
価格(JPY)
-
数量:
1 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS3248-05-3
IUPAC Name4,7-dimethyl-1,10-phenanthroline
Molecular FormulaC14H12N2
InChI KeyJIVLDFFWTQYGSR-UHFFFAOYSA-N
SMILESCC1=C2C=CC3=C(C)C=CN=C3C2=NC=C1
さらに表示
FormPowder
Assay (GC)≥97.5%
Appearance (Color)White to cream to pale brown
4,7-Dimethyl-1,10-phenanthroline acts as an intermediate in synthetic chemistry and dyestuff field. It is also used as an organic bidentate ligand and form complexes with metal for detection. Further, it plays an important role in colorimetric sensors, coordination polymer, ionochromism and luminescence.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4,7-Dimethyl-1,10-phenanthroline acts as an intermediate in synthetic chemistry and dyestuff field. It is also used as an organic bidentate ligand and form complexes with metal for detection. Further, it plays an important role in colorimetric sensors, coordination polymer, ionochromism and luminescence.

Solubility
Soluble in benzene and alcohol. Slightly soluble in water.

Notes
Incompatible with strong oxidizing agents and acids.
RUO – Research Use Only

General References:

  1. Murai, M.; Takami, K.; Takai, K. Iridium-Catalyzed Intermolecular Dehydrogenative Silylation of Polycyclic Aromatic Compounds without Directing Groups. Chem. Eur. J. 2015, 21 (12), 4566-4570.
  2. Carter, K. P.; Kalaj, M.; Cahill, C. L. Probing the Influence of N-Donor Capping Ligands on Supramolecular Assembly in Molecular Uranyl Materials. Eur. J. Inorg. Chem. 2016, 2016 (1), 126-137.