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Sigma-Aldrich

4,5-Diazafluoren-9-one

97%

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About This Item

Empirical Formula (Hill Notation):
C11H6N2O
CAS Number:
50890-67-0
Molecular Weight:
182.18
MDL number:
MFCD00046892
UNSPSC Code:
12352100
PubChem Substance ID:
24863238
NACRES:
NA.22

Quality Level

100

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

Related Categories

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Photoinduced energy-and electron-transfer processes in dinuclear ruthenium (II) and/or osmium (II) complexes connected by a linear rigid bis-chelating bridge.
De Cola L, et al.
Rec. Trav. Chim., 114(11-12), 534-541 (1995)
Ghulam A Shabir
Journal of chromatographic science, 46(7), 643-648 (2008-08-23)
A new liquid chromatography-mass spectrometry (LC-MS) method is developed and validated for the identification and determination of novel 4,5-diazafluoren-9-one compound. The method employs a Waters XTerra RP-18 column (150 mmx4.6 mm, i.d. 5 microm) with a mobile phase comprised of
4, 5-Diazafluoren-9-one.
Fun H-K, et al.
Acta Crystallographica Section C, Structural Chemistry, 51(10), 2076-2078 (1995)
4,5-Diazafluoren-9-one.
White PB and Stahl SS.
e-EROS Encyclopedia of Reagents for Organic Synthesis., 1-3 (2014)
Youxiang Wang et al.
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
View All Related Papers

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