F1506

9-Fluorenone

98%

• Synonym(s): 9H-Fluorene-9-one, Fluoren-9-one (8CI)
• Empirical Formula (Hill Notation): C₁₃H₈O
• CAS Number: 486-25-9
• Molecular Weight: 180.20
• Beilstein/REAXYS Number: 1636531
• EC Number: 207-630-7
• MDL number: MFCD00001141
• UNSPSC Code: 12352100
• PubChem Substance ID: 24894771
• NACRES: NA.22

Properties

• Quality Level: 200
• assay: 98%
• bp: 342 °C (lit.)
• mp: 80-83 °C (lit.)
• SMILES string: O=C1c2ccccc2-c3ccccc13
• InChI: 1S/C13H8O/c14-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8H
• InChI key: YLQWCDOCJODRMT-UHFFFAOYSA-N

Description

Application

9-Fluorenone has been extensively used as a precursor to synthesize a variety of organic electronic materials.[1][2][3] Some of the general examples are:

• Synthesis of host for the blue and green phosphorescent organic light emitting diodes (PHOLEDs).[1][2][4]
• Synthesis of fluorene-based molecular motors.[5]
• Synthesis of open-shell Chichibabin′s hydrocarbons as potential organic spintronic materials.[3]
• It also acts as a sensitizer in the formation of picene via photosensitization of 1,2-di(1-naphthyl)ethane.[6]

Safety Information

• pictograms: GHS07,GHS09
• signalword: Warning
• hcodes: H319,H411
• pcodes: P264 - P273 - P280 - P305 + P351 + P338 - P337 + P313 - P391
• Hazard Classifications: Aquatic Chronic 2 - Eye Irrit. 2
• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: 325.4 °F
• flash_point_c: 163 °C
• ppe: Eyeshields, Gloves, type N95 (US)