103068-20-8

  • Product Name1-Bromo-3,5-diphenylbenzene
  • Molecular FormulaC18H13Br
  • Molecular Weight309.2
  • Purity99%
Inquiry

Product Details

Quick Details

  • CasNo: 103068-20-8
  • Molecular Formula: C18H13Br
  • Purity: 99%

High Purity 1-Bromo-3,5-diphenylbenzene 103068-20-8 Good Price

  • Molecular Formula:C18H13Br
  • Molecular Weight:309.205
  • Melting Point:105-106℃ 
  • Boiling Point:401.13 °C at 760 mmHg 
  • Flash Point:192.162 °C 
  • PSA:0.00000 
  • Density:1.309 g/cm3 
  • LogP:5.78310 

1-Bromo-3,5-diphenylbenzene(Cas 103068-20-8) Usage

Chemical Properties

off-whtie powder

Uses

1-Bromo-3,5-diphenylbenzene is used in the synthesis of Aromatic Dendrimers Bearing 2,4,6-Triphenyl-1,3,5-triazine Cores.

InChI:InChI=1S/C18H13Br/c19-18-12-16(14-7-3-1-4-8-14)11-17(13-18)15-9-5-2-6-10-15/h1-13H

103068-20-8 Relevant articles

Highly efficient dual anthracene core derivatives through optimizing side groups for blue emission

Lee, Hayoon,Jo, Minjin,Yang, Garam,Jung, Hyocheol,Kang, Seokwoo,Park, Jongwook

, p. 27 - 36 (2017)

TP-AA-TPB, TP-AA-TPB, TPB-AA-TPB, TP-AA-...

A practical and efficient synthesis of 5′-substituted m-terphenyls

Kehlbeck, Joanne D.,Dimise, Eric J.,Sparks, Sarah M.,Ferrara, Skylar,Tanski, Joseph M.,Anderson, Craig M.

, p. 1979 - 1983 (2007)

Outlined is a simple, convenient, scalab...

Palladium Nanoparticles Supported on Poly(N-vinyl- imidazole-co-N-vinylcaprolactam) as an Effective Recyclable Catalyst for the Suzuki Reaction

Selivanova, Alexandra V.,Tyurin, Vladimir S.,Beletskaya, Irina P.

, p. 1278 - 1283 (2014)

A recyclable and effective polymer-immob...

Synthesis of a new, bulky tetraarylphosphonium, a tetraarylborate, and their salt

Matsumoto, Kaya,Hatano, Keiichiro,Umezawa, Naoki,Higuchi, Tsunehiko

, p. 2181 - 2185 (2004)

Tris(m-terphenyl-5′-yl)phosphine (2), te...

Synthesis and physical properties of new pyrene derivative with bulky side groups for blue emission

Jung, Mina,Lee, Jaehyun,Jung, Hyocheol,Park, Jongwook

, p. 8796 - 8799 (2016)

Organic light-emitting diodes (OLEDs) ha...

Catalytic formal cycloadditions between anhydrides and ketones: Excellent enantio and diastereocontrol, controllable decarboxylation and the formation of adjacent quaternary stereocentres

Cornaggia, Claudio,Gundala, Sivaji,Manoni, Francesco,Gopalasetty, Nagaraju,Connon, Stephen J.

, p. 3040 - 3046 (2016)

It has been shown for the first time tha...

Three-Dimensional Structures Based on the Fusion of Chrysene and Spirobifluorene Chromophores for the Development of Blue OLEDs

Lee, Hayoon,Jung, Hyocheol,Kang, Seokwoo,Heo, Jin Hyuck,Im, Sang Hyuk,Park, Jongwook

, p. 2640 - 2646 (2018)

A new deep-blue chromophore containing a...

Highly efficient pyrene blue emitters for OLEDs based on substitution position effect

Jung, Mina,Lee, Jaehyun,Jung, Hyocheol,Kang, Seokwoo,Wakamiya, Atsushi,Park, Jongwook

, p. 42 - 49 (2018)

To investigate the effect of substitutio...

In-Line Monitoring and Spectral Analysis of Polymer Blend Dispersion in Microcompounder

Oh, Won Taek,Kim, Myung Ho,Do, Quyen,Cho, Namchul,Kim, Tae-Dong

, p. 75 - 81 (2019)

Microcompounders are the most common com...

METHOD OF PRODUCING HALOGEN COMPOUND

-

Paragraph 0052-0060; 0079-0081, (2021/05/07)

PROBLEM TO BE SOLVED: To provide a metho...

Palladium-catalysed room-temperature Suzuki–Miyaura coupling in water extract of pomegranate ash, a bio-derived sustainable and renewable medium

Appa, Rama Moorhy,Prasad, S. Siva,Lakshmidevi, Jangam,Naidu, Bandameeda Ramesh,Narasimhulu, Manchala,Venkateswarlu, Katta

, (2019/08/12)

An agro waste-derived, ‘water extract of...

Preparation method of 3,5-diphenylbromobenzene

-

Paragraph 0019; 0021; 0022; 0024; 0025; 0027, (2019/07/01)

The invention belongs to the field of or...

103068-20-8 Process route

1,3,5-trisbromobenzene
626-39-1

1,3,5-trisbromobenzene

phenylboronic acid
98-80-6

phenylboronic acid

1,3,5-triphenylbenzene
612-71-5

1,3,5-triphenylbenzene

3,5-dibromo-1,1′-biphenyl
16372-96-6

3,5-dibromo-1,1′-biphenyl

1-bromo-3,5-diphenylbenzene
103068-20-8

1-bromo-3,5-diphenylbenzene

Conditions
Conditions Yield
With potassium carbonate; palladium dichloride; In ethanol; water; at 80 ℃; for 10h; Inert atmosphere;
6%
14%
62%
With palladium diacetate; In ethanol; at 20 ℃; for 0.25h;
33%
39%
17%
1,3,5-trisbromobenzene
626-39-1

1,3,5-trisbromobenzene

1,3-dibromo-5-iodobenzene
19752-57-9

1,3-dibromo-5-iodobenzene

phenylboronic acid
98-80-6

phenylboronic acid

1,3,5-triphenylbenzene
612-71-5

1,3,5-triphenylbenzene

3,5-dibromo-1,1′-biphenyl
16372-96-6

3,5-dibromo-1,1′-biphenyl

1-bromo-3,5-diphenylbenzene
103068-20-8

1-bromo-3,5-diphenylbenzene

Conditions
Conditions Yield
With palladium diacetate; In ethanol; at 20 ℃; for 0.25h;
12%
21%
51%

103068-20-8 Upstream products

  • 21521-51-7
    21521-51-7

    2,4,6-tribromoiodobenzene

  • 28023-86-1
    28023-86-1

    3,5-diphenylphenol

  • 63006-66-6
    63006-66-6

    N'-phenyl-(1,1';3',1'-terphenyl)-5'-amine

  • 626-39-1
    626-39-1

    1,3,5-trisbromobenzene

103068-20-8 Downstream products

  • 118357-13-4
    118357-13-4

    3,6-bis(3,5-diphenylphenyl)-1,2,3,6,7,8-hexahydro-4,5-dimethoxy-as-indacene-3,6-diol

  • 1036378-83-2
    1036378-83-2

    2-([1,1':3′,1''-terphenyl]-5'-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Relevant Products