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894791-46-9

  • Product Name9-[1,1'-Biphenyl-4-yl]-3-bromo-9h-carbazole
  • Molecular FormulaC24H16BrN
  • Molecular Weight398.3
  • Purity99%
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Product Details

Quick Details

  • CasNo： 894791-46-9
  • Molecular Formula： C24H16BrN
  • Purity： 99%

High Purity 9-[1,1'-Biphenyl-4-yl]-3-bromo-9H-carbazole 894791-46-9 In Stock

  • Molecular Formula:C24H16BrN
  • Molecular Weight:398.302
  • Melting Point:152-155°C 
  • Boiling Point:551.972 °C at 760 mmHg 
  • Flash Point:287.622 °C 
  • PSA：4.93000 
  • Density:1.329 g/cm3 
  • LogP:7.21320 

9-[1,1'-Biphenyl-4-yl]-3-bromo-9H-carbazole(Cas 894791-46-9) Usage

Chemical Properties

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

 

894791-46-9 Relevant articles

Organic compound, and organic electroluminescent device and electronic device using the same

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Paragraph 0129-0131; 0132; 0135, (2021/11/10)

The present invention relates to an orga...

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...

Organic electroluminescent material, electronic device and electronic apparatus

-

Paragraph 0145-0147, (2020/05/02)

The present application relates to an or...

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

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Paragraph 0053-0056; 0099, (2020/12/14)

The invention relates to a method for sy...

894791-46-9 Process route

3-bromo-9H-carbazole
1592-95-6

3-bromo-9H-carbazole

4-iodo-biphenyl
1591-31-7

4-iodo-biphenyl

9-[1,1′-biphenyl-4-yl]-3-bromo-9H-carbazole
894791-46-9

9-[1,1′-biphenyl-4-yl]-3-bromo-9H-carbazole

Conditions
Conditions Yield
With tris-(dibenzylideneacetone)dipalladium(0); tributylphosphine; In toluene; for 12h; Heating;
87.6%
With copper(l) iodide; potassium carbonate; o-phenanthroline; In N,N-dimethyl-formamide; at 155 ℃; Inert atmosphere;
78%
With copper(l) iodide; 1,10-Phenanthroline; 18-crown-6 ether; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; at 130 - 135 ℃; for 7h; Inert atmosphere;
477.96 g
3-bromo-9H-carbazole
1592-95-6

3-bromo-9H-carbazole

biphenyl-4-yl-hydrazine
2217-77-8

biphenyl-4-yl-hydrazine

9-[1,1′-biphenyl-4-yl]-3-bromo-9H-carbazole
894791-46-9

9-[1,1′-biphenyl-4-yl]-3-bromo-9H-carbazole

Conditions
Conditions Yield
With potassium carbonate; copper(l) chloride; In acetonitrile; at 0 ℃; for 4h; Schlenk technique;
95%

894791-46-9 Upstream products

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    6299-16-7

    9-([1,1’-biphenyl]-4-yl)-9H-carbazole

  • 92-66-0
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    4-bromo-1,1'-biphenyl

  • 86-74-8
    86-74-8

    9H-carbazole

  • 1592-95-6
    1592-95-6

    3-bromo-9H-carbazole

894791-46-9 Downstream products

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    1028648-22-7

    9‐{[1,1'‐biphenyl]‐4‐yl}carbazol‐3‐ylboronic acid

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    C42H28N2

  • 1643479-47-3
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    9-([1,1'-biphenyl]-3-yl)-9’-([1,1'-biphenyl]-4-yl)-9H,9'H-3,3'-bicarbazole

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