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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

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

-

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...

ORGANIC MIXTURE, COMPOSITION, AND ORGANIC ELECTRONIC COMPONENT

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Paragraph 0199, (2020/01/03)

Disclosed in the present application is ...

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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