1428551-28-3

  • Product Name9-([1,1'-Biphenyl]-3-yl)-3-bromo-9h-carbazole
  • Molecular FormulaC24H16BrN
  • Molecular Weight398.3
  • Purity99%
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Product Details

Quick Details

  • CasNo: 1428551-28-3
  • Molecular Formula: C24H16BrN
  • Purity: 99%

High Quality Pharmaceutical Intermediates 1428551-28-3 9-([1,1'-biphenyl]-3-yl)-3-broMo-9H-carbazole

  • Molecular Formula:C24H16BrN
  • Molecular Weight:398.302
  • Melting Point:108.0 to 112.0 °C 
  • Boiling Point:570.3±42.0 °C(Predicted) 
  • PSA:4.93000 
  • Density:1.32±0.1 g/cm3(Predicted) 
  • LogP:7.21320 

9-([1,1'-biphenyl]-3-yl)-3-broMo-9H-carbazole(Cas 1428551-28-3) Usage

Description 9-([1,1'-Biphenyl]-3-yl)-3-bromo-9H-carbazole is an organic compound consists of a carbazole unit substituted with a 3-brominated biphenyl moiety. 9-([1,1'-Biphenyl]-3-yl)-3-bromo-9H-carbazole is a solid at room temperature and exhibits interesting photophysical and electronic properties, making it potentially useful in the field of organic electronics. The presence of the bromine substituent and the biphenyl group provides opportunities for further chemical functionalization and integration into various optoelectronic devices, such as organic light-emitting diodes (OLEDs), organic field-effect transistors (OFETs), and other advanced materials. The unique structural features of 9-([1,1'-biphenyl]-3-yl)-3-bromo-9H-carbazole contribute to its potential applications in areas like organic semiconductors, photovoltaics, and luminescent materials.

Application

9-([1,1'-Biphenyl]-3-yl)-3-bromo-9H-carbazole (cas# 1428551-28-3) is used as the OLED.

XLogP3-AA 7.3
Complexity 473

Isomeric SMILES: C1=CC=C(C=C1)C2=CC(=CC=C2)N3C4=C(C=C(C=C4)Br)C5=CC=CC=C53  
InChIKey: NSRPRPVECXNOLB-UHFFFAOYSA-N  
InChI: InChI=1S/C24H16BrN/c25-19-13-14-24-22(16-19)21-11-4-5-12-23(21)26(24)20-10-6-9-18(15-20)17-7-2-1-3-8-17/h1-16H  

1428551-28-3 Relevant articles

Organic electroluminescent host material and application thereof in organic electroluminescent device

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Paragraph 0049; 0053-0055, (2021/07/17)

The invention relates to an organic elec...

COMPOUND FOR ORGANIC ELECTRONIC ELEMENT, ORGANIC ELECTRONIC ELEMENT USING THE SAME, AND AN ELECTRONIC DEVICE THEREOF

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Paragraph 0125-0128; 0129-0130; 0133, (2021/02/16)

An object of the present invention is to...

Method for synthesizing N-aryl carbazole compound by catalyzing reaction of carbazole with aryl hydrazine by using transition metal

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Paragraph 0065-0068; 0100, (2020/12/14)

The invention relates to a method for sy...

1428551-28-3 Process route

9-([1,1'-biphenyl]-3-yl)-9H-carbazole
1221237-87-1

9-([1,1'-biphenyl]-3-yl)-9H-carbazole

9-([1,1′-biphenyl]-3-yl)-3-bromo-9H-carbazole
1428551-28-3

9-([1,1′-biphenyl]-3-yl)-3-bromo-9H-carbazole

Conditions
Conditions Yield
With N-Bromosuccinimide; In N,N-dimethyl-formamide; for 12h; Reflux;
90%
With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
88%
With N-Bromosuccinimide; In N,N-dimethyl-formamide; for 12h; Cooling with ice; Darkness;
88%
With N-Bromosuccinimide; In chloroform; for 5h; Reflux;
 
With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20 ℃; for 12h;
40 g
With N-Bromosuccinimide; at 20 ℃;
 
3-bromo-9H-carbazole
1592-95-6

3-bromo-9H-carbazole

3-iodo-1,1'-biphenyl
20442-79-9

3-iodo-1,1'-biphenyl

9-([1,1′-biphenyl]-3-yl)-3-bromo-9H-carbazole
1428551-28-3

9-([1,1′-biphenyl]-3-yl)-3-bromo-9H-carbazole

Conditions
Conditions Yield
With tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine; sodium t-butanolate; In toluene; at 100 ℃;
84%
With tri-tert-butyl phosphine; bis(dibenzylideneacetone)-palladium(0); sodium t-butanolate; In toluene; at 100 ℃; for 10h; Inert atmosphere;
51%

1428551-28-3 Upstream products

  • 1592-95-6
    1592-95-6

    3-bromo-9H-carbazole

  • 20442-79-9
    20442-79-9

    3-iodo-1,1'-biphenyl

  • 1221237-87-1
    1221237-87-1

    9-([1,1'-biphenyl]-3-yl)-9H-carbazole

  • 185112-61-2
    185112-61-2

    9-(3-bromophenyl)carbazole

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