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Quality Level
Assay
97%
mp
214-217 °C (lit.)
solubility
THF: soluble(lit.)
benzene: soluble(lit.)
dichloromethane: soluble(lit.)
toluene: soluble(lit.)
SMILES string
O=C1c2cccnc2-c3ncccc13
InChI
1S/C11H6N2O/c14-11-7-3-1-5-12-9(7)10-8(11)4-2-6-13-10/h1-6H
InChI key
PFMTUGNLBQSHQC-UHFFFAOYSA-N
General description
4,5-Diazafluoren-9-one is a heterocyclic building block used in the synthesis of various heterocyclic compounds and also as a fluorescent probe.
Application
4,5-Diazafluoren-9-one may be used in the preparation of heterocyclic ligands, by condensation with various diamines, hydrazine, 1,4-phenylenediamine, benzidine and 4,4′-methylenedianiline. It may be used in the preparation of 9-diazo-4,5-diazafluorene.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
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4, 5-Diazafluoren-9-one from the oxidation of 1, 10-phenanthroline by permanganate.
Australian Journal of Chemistry, 26(12), 2727-2728 (1973)
4, 5-Diazafluoren-9-one.
Acta Crystallographica Section C, Crystal Structure Communications, 51(10), 2076-2078 (1995)
Inorganic chemistry, 37(9), 2227-2234 (2001-10-24)
A series of bimetallic complexes of ruthenium(II) bridged by heterocyclic ligands formed by the condensation of 4,5-diazafluoren-9-one with various diamines, hydrazine, 1,4-phenylenediamine, benzidine, and 4,4'-methylenedianiline, results in metal centers separated by various distances. The complexes give rise to metal-to-ligand charge-transfer
4,5-Diazafluoren-9-one.
e-EROS Encyclopedia of Reagents for Organic Synthesis., 1-3 (2014)
Synthesis and Application of New Ru (II) Complexes for Dye-Sensitized Nanocrystalline TiO2 Solar Cells.
Bull. Korean Chem. Soc., 28(8), 1311-1311 (2011)
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