400607-16-1

  • Product NameAnthracene, 9-[1,1'-biphenyl]-2-yl-10-bromo-
  • Purity99%
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Product Details

Quick Details

  • CasNo: 400607-16-1
  • Purity: 99%

400607-16-1 Properties

  • Molecular Formula:C26H17Br
  • Molecular Weight:409.325
  • Melting Point:146.0 to 150.0 °C 
  • Boiling Point:508.6±19.0 °C(Predicted) 
  • PSA:0.00000 
  • Density:1.344±0.06 g/cm3(Predicted) 
  • LogP:8.08950 

400607-16-1 Usage

Chemical Properties

yellow powder

400607-16-1 Relevant articles

Compound, organic luminescent material and organic electroluminescent device

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Paragraph 00175; 00176; 00178, (2021/08/19)

The invention provides a compound as shown in a general formula (I), which has a mother structure of sym-triphenyl substituted anthracene, is high in bond energy among atoms, has good thermal stability, is beneficial to solid-state accumulation among molecules, is large in bandwidth, has a light-emitting region in a blue light region, is high in light-emitting intensity, and has a proper energy level with adjacent levels. And injection and migration of excitons are facilitated. When the compound is used as a blue light host material in a luminescent layer, the driving voltage of an organic electroluminescent device can be effectively reduced, the luminous efficiency is improved, and the service life is prolonged. The invention also provides an organic electroluminescent device and a display device containing the compound of the general formula (I).

Novel compound and organic light emitting device comprising the same

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Paragraph 0158; 0163-0165; 0171-0173, (2021/03/09)

The present invention provides a novel compound and an organic light emitting device using the same. The present invention provides a compound represented by chemical formula 1. The compound represented by chemical formula 1 described above can be used as a material for an organic layer of the organic light emitting device, and can improve efficiency, low driving voltage, and/or lifespan characteristics in the organic light emitting device.

Organic compound and electronic element and electronic device using same (by machine translation)

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Paragraph 0140-0143; 0146, (2021/01/15)

The invention belongs to the technical field of organic materials, and particularly relates to an organic compound and an electronic element and an electronic device using the same, wherein the organic compound has the structure shown 1. When the compound is used as an electron transport layer for preparing an organic electroluminescent device, the service life of the organic electroluminescent device can be effectively prolonged, and the luminous efficiency or the driving voltage can be improved to a certain extent. (by machine translation)

Naphthyl benzofuran and anthracene derivative, preparation method and application thereof and device

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, (2018/07/10)

The invention belongs to the field of application sciences of organic photoelectric materials and specifically relates to a naphthyl benzofuran and anthracene derivative, a preparation method and application thereof and a device. The naphthyl benzofuran a

400607-16-1 Process route

9‐([1,1'‐biphenyl]‐2‐yl)anthracene
849223-96-7

9‐([1,1'‐biphenyl]‐2‐yl)anthracene

9-([1,1′-biphenyl]-2-yl)-10-bromoanthracene
400607-16-1

9-([1,1′-biphenyl]-2-yl)-10-bromoanthracene

Conditions
Conditions Yield
With N-Bromosuccinimide; In chloroform; N,N-dimethyl-formamide; at 40 ℃; for 12h; Inert atmosphere;
90%
With N-Bromosuccinimide; In dichloromethane; at 20 ℃; for 2h; Darkness;
With N-Bromosuccinimide; In dichloromethane; at 0 ℃; for 4h;
2-Bromobiphenyl
2052-07-5

2-Bromobiphenyl

9-([1,1′-biphenyl]-2-yl)-10-bromoanthracene
400607-16-1

9-([1,1′-biphenyl]-2-yl)-10-bromoanthracene

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1.1: n-butyllithium / hexane; tetrahydrofuran / -78 °C
1.2: -78 - 20 °C
2.1: sodium carbonate / tetrakis(triphenylphosphine) palladium(0) / toluene; water / 3 h / 100 °C
3.1: N-Bromosuccinimide / dichloromethane / 2 h / 20 °C / Darkness
With N-Bromosuccinimide; n-butyllithium; sodium carbonate; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; hexane; dichloromethane; water; toluene;
Multi-step reaction with 2 steps
1: potassium carbonate; tetrakis(triphenylphosphine) palladium(0) / tetrahydrofuran / 12 h / Inert atmosphere; Sonication
2: N-Bromosuccinimide / chloroform; N,N-dimethyl-formamide / 12 h / 40 °C / Inert atmosphere
With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;

400607-16-1 Upstream products

  • 2052-07-5
    2052-07-5

    2-Bromobiphenyl

  • 914675-52-8
    914675-52-8

    2‐{[1,1'‐biphenyl]‐2‐yl}‐4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolane

  • 849223-96-7
    849223-96-7

    9‐([1,1'‐biphenyl]‐2‐yl)anthracene

  • 100622-34-2
    100622-34-2

    anthracene-9-boronic acid

400607-16-1 Downstream products

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    C32H29BO2

  • 400607-48-9
    400607-48-9

    10-([1,1'-biphenyl]-2-yl)-9-anthracenylboronic acid