Identification | More | [Name]
2,7-Dibromo-9,9-dimethylfluorene | [CAS]
28320-32-3 | [Synonyms]
9,9-Dimethyl-2,7-dibromofluorenone 2,7-Dibromo-9,9-dimethyl-fluororene 2,7-Dibromo-9,9-dimethylfluorene 9H-Fluorene,2,7-dibromo-9,9-dimethyl- | [EINECS(EC#)]
640-177-7 | [Molecular Formula]
C15H12Br2 | [MDL Number]
MFCD00099471 | [Molecular Weight]
352.06 | [MOL File]
28320-32-3.mol |
Chemical Properties | Back Directory | [Melting point ]
180°C | [Boiling point ]
401.8±38.0 °C(Predicted) | [density ]
1.606±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
soluble in Toluene | [form ]
powder | [color ]
White to Light yellow to Light orange | [InChIKey]
LONBOJIXBFUBKQ-UHFFFAOYSA-N | [CAS DataBase Reference]
28320-32-3(CAS DataBase Reference) |
Questions And Answer | Back Directory | [Synthesis]
(1) In a 250 mL single-necked flask was added 2,7-dibromofluorene (9.72 g, 30 mmol), tetra-n-butylammonium bromide (0.08 g, 0.25 mmol), iodomethane (12.8 g, 90 mmol), 10 mL of NaOH solution, and 120 mL of DMSO.The mixture was allowed to react for 5 hours under ultrasonic conditions (100 W). After completion of the reaction, the reaction solution was poured into 500 mL of water, pumped and filtered for 30 min, the filter cake was washed with water and dried to give 10.5 g of light yellow solid in 99% yield. references: [1] Patent: CN106349163, 2017, A. Location in patent: Paragraph 0080; 0081; 0099; 0100; 0113; 0114 [2] Patent: CN108409668, 2018, A. Location in patent: Paragraph 0075-0076; 0078 [3] Patent: EP1860097, 2007, A1. Location in patent: Page/Page column 21; 22 [4] Patent: US8058450, 2011, B2. Location in patent: Page/Page column 43 [5] Journal of Organic Chemistry, 2004, vol. 69, # 3, p. 987 - 990 |
Hazard Information | Back Directory | [Chemical Properties]
White solid | [Uses]
This material is a precursor to a number of organic semiconducting polymers for OPV as well as a variety of hole transport for OLED devices. |
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