2-bromo-9-fluorenone

Names

[ Name ]:
2-bromo-9-fluorenone

[Synonym ]:
MFCD00010789
2-bromanylfluoren-9-one
2-bromo-fluoren-9-one
9H-Fluoren-9-one, 2-bromo-
2-bromofluorenone-9
2-bromofluoreneone
2-Bromo-9H-fluoren-9-one
2-BroMo-9-fluorenone
2-bromofluorenone

Chemical & Physical Properties

[ Density]:
1.6±0.1 g/cm3

[ Boiling Point ]:
392.8±21.0 °C at 760 mmHg

[ Melting Point ]:
146-148 °C(lit.)

[ Molecular Formula ]:
C₁₃H₇BrO

[ Molecular Weight ]:
259.098

[ Flash Point ]:
131.3±9.4 °C

[ Exact Mass ]:
257.968018

[ PSA ]:
17.07000

[ LogP ]:
4.35

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.691

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2914700090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2914700090

[ Summary ]:
HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

Articles

Supramolecular luminescence from oligofluorenol-based supramolecular polymer semiconductors.

Int. J. Mol. Sci. 14 , 22368-79, (2013)

Supramolecular luminescence stems from non-covalent exciton behaviors of active π-segments in supramolecular entities or aggregates via intermolecular forces. Herein, a π-conjugated oligofluorenol, co...

Towards dynamic control of wettability by using functionalized altitudinal molecular motors on solid surfaces.

Chemistry 19(32) , 10690-7, (2013)

We report the synthesis of altitudinal molecular motors that contain functional groups in their rotor part. In an approach to achieve dynamic control over the properties of solid surfaces, a hydrophob...

Oxidative stability and its effect on the photoluminescence of poly (fluorene) derivatives: end group effects. Lee J-I, et al.

Chem. Mater. 11(4) , 1083-88, (1999)