78600-31-4

  • Product Name:2-BromoTriphenylamine
  • Molecular Formula:C18H14BrN
  • Purity:99%
  • Molecular Weight:324.22
Inquiry

Product Details

pd_meltingpoint:61.0 to 65.0 °C

Purity:99%

Quality Manufacturer Supply High Purity 99% 2-BromoTriphenylamine 78600-31-4 with Reasonable Price

  • Molecular Formula:C18H14BrN
  • Molecular Weight:324.22
  • Melting Point:61.0 to 65.0 °C 
  • Boiling Point:165°C/0.3mmHg(lit.) 
  • PKA:-3.76±0.18(Predicted) 
  • PSA:3.24000 
  • Density:1.369 
  • LogP:5.91890 

78600-31-4 Relevant articles

Construction of a Polycyclic Conjugated System Containing a Dibenzazepine Moiety by Cationic Gold(I)-Catalyzed Cycloisomerization

Ito, Mamoru,Kawasaki, Ryosuke,Kanyiva, Kyalo Stephen,Shibata, Takanori

, p. 5234 - 5237 (2016)

A new π-conjugated system of nitrogen-co...

Efficient synthesis of π-extended phenazasilines for optical and electronic applications

Li, Huanhuan,Wang, Yang,Yuan, Kai,Tao, Ye,Chen, Runfeng,Zheng, Chao,Zhou, Xinhui,Li, Junfeng,Huang, Wei

, p. 15760 - 15763 (2014)

The rhodium-catalyzed synthesis of phena...

A novel spiro-annulated benzimidazole host for highly efficient blue phosphorescent organic light-emitting devices

Chen, Wen-Cheng,Yuan, Yi,Zhu, Ze-Lin,Ni, Shao-Fei,Jiang, Zuo-Quan,Liao, Liang-Sheng,Wong, Fu-Lung,Lee, Chun-Sing

, p. 4541 - 4544 (2018)

A novel host material featuring a spiro-...

Highly efficient dual-core derivatives with EQEs as high as 8.38% at high brightness for OLED blue emitters

Kang, Seokwoo,Jung, Hyocheol,Lee, Hayoon,Park, Sunwoo,Kim, Joonghan,Park, Jongwook

, p. 14709 - 14716 (2019/12/06)

Three blue fluorescent materials were ne...

Organic metal compounds and organic light emitting diodes comprising the same

-

Paragraph 0145; 0148-0151, (2018/10/19)

PURPOSE: An organic metal compound and a...

COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE DEVICES, ORGANIC ELECTROLUMINESCENCE DEVICE, AND ELECTRONIC DEVICE

-

Paragraph 0204, (2018/07/15)

A compound represented by formula (1): w...

78600-31-4 Process route

1-Bromo-2-iodobenzene
583-55-1

1-Bromo-2-iodobenzene

diphenylamine
122-39-4

diphenylamine

N-(2-bromophenyl)-N-phenylbenzenamine
78600-31-4

N-(2-bromophenyl)-N-phenylbenzenamine

Conditions
Conditions Yield
With potassium carbonate; copper dichloride; In dimethyl sulfoxide; for 12h; Reflux;
83.7%
With tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine; sodium t-butanolate; In toluene; at 100 ℃;
76%
With tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine; sodium t-butanolate; In toluene; at 100 ℃;
76%
With tris-(dibenzylideneacetone)dipalladium(0); triphenylphosphine; sodium t-butanolate; In toluene; at 100 ℃;
76%
With palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; sodium t-butanolate; In toluene; at 100 ℃; for 12h; chemoselective reaction; Inert atmosphere;
75%
With palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; sodium t-butanolate; In toluene; for 1h; Inert atmosphere; Schlenk technique; Heating;
74%
With palladium diacetate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; sodium t-butanolate; In toluene; at 100 ℃; for 12h; Green chemistry;
74%
With copper; potassium carbonate; In various solvent(s); for 96h; Heating;
69%
With potassium phosphate; copper(l) iodide; N,N`-dimethylethylenediamine; In 5,5-dimethyl-1,3-cyclohexadiene; at 120 ℃; for 48h;
55%
With copper(l) iodide; 1,10-Phenanthroline; potassium hydroxide; In toluene; Inert atmosphere; Reflux;
52%
With tri-tert-butyl phosphine; palladium diacetate; sodium t-butanolate; In toluene; at 110 ℃; for 24h; Inert atmosphere;
51%
With potassium hydroxide; 1,10-Phenanthroline; In toluene; at 125 ℃;
37%
With copper(l) iodide; potassium carbonate; In o-xylene; at 120 ℃;
37.3%
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; at 120 ℃; Reflux;
37.3%
With copper(l) iodide; potassium carbonate; In para-xylene; for 24h; Reflux;
30%
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; at 120 ℃; for 48h;
Inert atmosphere;
With tri-tert-butyl phosphine; palladium diacetate; sodium t-butanolate; In toluene;
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene;
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene;
With copper(l) iodide; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene;
diphenylamine
122-39-4

diphenylamine

2,3-dibromobenzene
583-53-9

2,3-dibromobenzene

N-(2-bromophenyl)-N-phenylbenzenamine
78600-31-4

N-(2-bromophenyl)-N-phenylbenzenamine

Conditions
Conditions Yield
With copper(l) iodide; 18-crown-6 ether; In 1,2-dichloro-benzene; at 100 - 210 ℃; Inert atmosphere; Darkness;
73%

78600-31-4 Upstream products

  • 583-55-1
    583-55-1

    1-Bromo-2-iodobenzene

  • 122-39-4
    122-39-4

    diphenylamine

  • 583-53-9
    583-53-9

    2,3-dibromobenzene

78600-31-4 Downstream products

  • 615564-54-0
    615564-54-0

    1-(Ph2N)-2-[B(C6F5)2]C6H4

  • 1416947-05-1
    1416947-05-1

    10-phenyl-2',7'-bis(triphenylsilyl)-10H-spiro[acridine-9,9'-fluorene]

  • 880800-04-4
    880800-04-4

    2',7'-dibromo-10-phenyl-10H-spiro[acridine-9,9'-fluorene]

  • 1467099-24-6
    1467099-24-6

    C43H27NS

Relevant Products