168646-54-6
168646-54-6
Chemical Structure
5,6-Diamino-1,10-phenanthroline
- CAS No.: 168646-54-6
- Formula:C12H10N4
- Molecular Weight:210.24
IUPAC Name: 1,10-phenanthroline-5,6-diamine
InChIKey: MNXMBMNXSPNINS-UHFFFAOYSA-N
SMILES: NC1=C(C=CC=N2)C2=C(N=CC=C3)C3=C1N
Biological Activity: 5,6-Diamino-1,10-phenanthroline is a heterocyclic synthetic building block with amino substituents at the 5- and 6-positions of the 1,10-phenanthroline parent ring, and can yield Schiff base ligands via condensation reactions. 5,6-Diamino-1,10-phenanthroline can be used as an intermediate in research related to organic synthesis[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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5,6-Diamino-1,10-phenanthroline | 97.42% | 5,6-Diamino-1,10-phenanthroline is a heterocyclic synthetic building block with amino substituents at the 5- and 6-positions of the 1,10-phenanthroline parent ring, and can yield Schiff base ligands via condensation reactions. 5,6-Diamino-1,10-phenanthroline can be used as an intermediate in research related to organic synthesis. | ||||||||||||||||||||
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References
- [1]. Shao J, et al. Enantioselectively generating imidazolone dIz by the chiral DNA intercalating and "light-switching" Ru(II) polypyridyl complex via a novel flash-quench method. Free radical biology & medicine. 2024 Nov 20;225:157-163.
- [2]. Sadi AH, et al. Synthesis, characterization and antimicrobial studies of Ru (II) complexes with Schiff base co-ligand derived from 5, 6-diamino-1, 10-phenanthroline and benzene-1, 4-dicarbaldehyde. Bayero Journal of Pure and Applied Sciences. 2017;10(1):468-76.
- [3]. Idris MI, et al. SYNTHESIS, CHARACTERIZATION AND BIOLOGICAL STUDIES OF NI (II) COMPLEXES WITH SCHIFF BASE CO-LIGAND DERIVED FROM 5, 6-DIAMINO-1, 10-PHENANTHROLINE AND BENZENE-1, 4-DICARBALDEHYDE. Fudma Journal of Sciences. 2020 Sep 12;4(3):132-41.
