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2-Bromo-9,9-bis(4-methylphenyl)-9H-fluorene is a chemical compound that belongs to the family of fluorenes, which are polycyclic aromatic hydrocarbons. It is a brominated derivative of 9,9-bis(4-methylphenyl)-9H-fluorene, characterized by its unique chemical structure and properties. 2-Bromo-9,9-bis(4-methylphenyl)-9H-fluorene is known for its potential applications in various fields, particularly in the realm of organic electronics and materials science.

474918-33-7

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474918-33-7 Usage

Uses

Used in Organic Synthesis:
2-Bromo-9,9-bis(4-methylphenyl)-9H-fluorene is used as a key intermediate in various organic synthesis reactions. Its unique structure allows for the formation of new compounds with desired properties, making it a valuable building block in the synthesis of complex organic molecules.
Used in Organic Light-Emitting Diodes (OLEDs):
In the field of organic electronics, 2-Bromo-9,9-bis(4-methylphenyl)-9H-fluorene is used as a component in the development of organic light-emitting diodes (OLEDs). Its optoelectronic properties contribute to the efficient emission of light in these devices, enhancing their performance and energy efficiency.
Used in Organic Photovoltaics:
2-Bromo-9,9-bis(4-methylphenyl)-9H-fluorene also finds application in the development of organic photovoltaics. Its optoelectronic characteristics make it suitable for use in solar cells, where it can help improve the conversion efficiency of sunlight into electricity.
Used in Organic Semiconductors:
2-Bromo-9,9-bis(4-methylphenyl)-9H-fluorene is utilized in the research and development of organic semiconductors. Its unique properties allow for the creation of materials with tailored electronic characteristics, which can be used in various electronic devices and applications.
Used in Materials Science:
2-Bromo-9,9-bis(4-methylphenyl)-9H-fluorene is employed in materials science for the development of new materials with specific properties. Its unique chemical structure and properties make it a valuable compound for research and development in this field, contributing to the advancement of novel materials with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 474918-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,9,1 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 474918-33:
(8*4)+(7*7)+(6*4)+(5*9)+(4*1)+(3*8)+(2*3)+(1*3)=187
187 % 10 = 7
So 474918-33-7 is a valid CAS Registry Number.

474918-33-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-9,9-bis(4-methylphenyl)fluorene

1.2 Other means of identification

Product number -
Other names 2-Bromo-9,9-di-p-tolyl-9H-fluorene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:474918-33-7 SDS

474918-33-7Relevant academic research and scientific papers

QUINOXALINE DERIVATIVES AND ORGANIC LIGHT-EMITTING DIODES COMPRISING THE SAME

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, (2012/12/14)

A quinoxaline derivative represented by Formula (I) of or Formula (II) of is provided. In Formula (I) or (II), R1, R2, R3 and R4 are, independently, hydrogen, halogen, methyl, ethyl, propyl, butyl, aryl or heteroaryl, for example phenyl, furyl, thienyl, pyridyl, pyrimidyl, benzothiazolyl or benzoimidazolyl. The disclosure also provides an organic light-emitting diode including the quinoxaline derivative.

Ter(9,9-diarylfluorene)s: Highly efficient blue emitter with promising electrochemical and thermal stability

Wong, Ken-Tsung,Chien, Yuh-Yih,Chen, Ruei-Tang,Wang, Chung-Feng,Lin, Yu-Ting,Chiang, Huo-Hsien,Hsieh, Ping-Yuan,Wu, Chung-Chih,Chou, Chung Hsien,Su, Yuhlong Oliver,Lee, Gene-Hsiang,Peng, Shie-Ming

, p. 11576 - 11577 (2007/10/03)

Novel ter(9,9-diarylfluorene)s were synthesized by a Suzuki-coupling reaction of 2-bromofluorene (1) and 2,7-fluorenediboronic ester derivatives (3) with high isolated yields (63-86%). The X-ray structure analysis of ter(9,9′-spirobifluorene) (4aa) revealed that the conjugated chromophore adopts a helical conformation. This conformation effectively releases the steric interaction between the fluorene moieties and prevents inter-chromophore interactions. The introduction of aryl groups at the C9 position of fluorene was highly beneficial to the thermal and morphological stability of these oligomers. These terfluorenes exhibit intense blue fluorescence with excellent quantum yields both in solution (~100%) and in solid state (66-90%), and possess interesting reversible redox properties. Highly efficient blue light-emitting OLED devices were fabricated using 4aa and 4cc as emitters as well as hole transporters. The devices exhibit low turn-on voltage (~3 V) and high EL external quantum efficiency (2.5-3%). Copyright

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