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7511-49-1

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7511-49-1 Usage

Description

1,3,5-Tris(4-bromophenyl)benzene (TBB) is a halogenated aromatic monomer characterized by its unique structure, which features three 4-bromophenyl groups attached to a central benzene ring. This structural composition endows TBB with specific properties that make it suitable for a variety of applications across different industries.

Uses

Used in Environmental Applications:
1,3,5-Tris(4-bromophenyl)benzene is used as a key component in the synthesis of porous aromatic frameworks (PAFs) for the development of adsorption membranes. These membranes are designed to effectively treat organic pollutants, making TBB a valuable asset in the field of environmental protection and pollution control.
Used in Electronics Industry:
1,3,5-Tris(4-bromophenyl)benzene is used as a crucial material in the fabrication of pyridine-based high-efficiency organic light-emitting diodes (OLEDs). The incorporation of TBB in OLEDs enhances their performance, leading to more efficient and longer-lasting devices, which is particularly beneficial in the rapidly advancing electronics and display technology sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 7511-49-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 1 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7511-49:
(6*7)+(5*5)+(4*1)+(3*1)+(2*4)+(1*9)=91
91 % 10 = 1
So 7511-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H15Br3/c25-22-7-1-16(2-8-22)19-13-20(17-3-9-23(26)10-4-17)15-21(14-19)18-5-11-24(27)12-6-18/h1-15H

7511-49-1 Well-known Company Product Price

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  • (Code)Product description
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  • Packaging
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  • Alfa Aesar

  • (H37636)  1,3,5-Tris(4-bromophenyl)benzene, 97%   

  • 7511-49-1

  • 1g

  • 522.0CNY

  • Detail
  • Alfa Aesar

  • (H37636)  1,3,5-Tris(4-bromophenyl)benzene, 97%   

  • 7511-49-1

  • 5g

  • 1925.0CNY

  • Detail
  • Aldrich

  • (648906)  1,3,5-Tris(4-bromophenyl)benzene  97%

  • 7511-49-1

  • 648906-1G

  • 939.51CNY

  • Detail
  • Aldrich

  • (648906)  1,3,5-Tris(4-bromophenyl)benzene  97%

  • 7511-49-1

  • 648906-5G

  • 2,909.79CNY

  • Detail

7511-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-Tris(4-bromophenyl)benzene

1.2 Other means of identification

Product number -
Other names 1,3,5-tris(4-bromophenyl)benzene

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:7511-49-1 SDS

7511-49-1Relevant articles and documents

Zirconocene bis(perfluorooctanesulfonate) s-catalyzed highly efficient synthesis of 1,3,5-triaryl benzene via cyclotrimerization of ketones

Zhang, Guo Ping,Qiu, Ren Hua,Xu, Xin Hua,Zhou, Hai Hui,Kuang, Ya Fei,Chen, Si Hai

experimental part, p. 858 - 864 (2012/01/19)

Air-stable zirconocene bis(perfluoroctanesulfonate) s [Cp 2Zr]OSO2C8F17) 2] (1) with high Lewis acidity and high thermal stability was prepared by the reaction between Cp2ZrCl2 a

A New Approach to the Stereoselective Synthesis of β-methylchalcones

Elmorsy, Saad S.,Khalil, Abdel Galel M.,Girges, M. M.,Salama, Tarek A.

, p. 1537 - 1544 (2007/10/03)

Many β-methylchalcone derivatives have been prepared from self condensation of aralkyl ketones mediated by tetrachlorosilane-ethanol in mild conditions. - Key words: aralkyl ketones; tetrachlorosilane; β-methylchalcones; triarylbenzene derivatives

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