32228-99-2

  • Product Name:N-Phenyl-4-biphenylamin
  • Molecular Formula:C18H15N
  • Purity:99%
  • Molecular Weight:245.324
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Product Details;

CasNo: 32228-99-2

Molecular Formula: C18H15N

Buy High Quality 99% Pure N-Phenyl-4-biphenylamin 32228-99-2 Safe Shipping

  • Molecular Formula:C18H15N
  • Molecular Weight:245.324
  • Vapor Pressure:5.68E-07mmHg at 25°C 
  • Melting Point:113 °C 
  • Refractive Index:1.646 
  • Boiling Point:411.2 °C at 760 mmHg 
  • PKA:0.73±0.20(Predicted) 
  • Flash Point:217.6 °C 
  • PSA:12.03000 
  • Density:1.111 g/cm3 
  • LogP:5.17020 

N-Phenyl-4-biphenylamine(Cas 32228-99-2) Usage

Uses

N-Phenyl-4-biphenylamine (cas# 32228-99-2) is a useful reagent for the preparation of heterocyclic compounds for organic electrical devices.

InChI:InChI=1/C18H15N/c1-3-7-15(8-4-1)16-11-13-18(14-12-16)19-17-9-5-2-6-10-17/h1-14,19H

32228-99-2 Relevant articles

Organic compound and electronic device and device containing the same

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Paragraph 0230; 0257-0259, (2021/09/11)

The invention relates to the technical f...

Organic compound, electronic device comprising organic compound and electronic equipment

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Paragraph 0116-0118, (2021/08/07)

The invention relates to an organic comp...

Organic compound and electronic component and electronic device comprising same

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Paragraph 0113-0115, (2021/07/17)

The invention provides an organic compou...

Organic compound, and electronic element and electronic device using same

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Paragraph 0150-0151, (2021/07/14)

The invention relates to an organic comp...

32228-99-2 Process route

bromobenzene
108-86-1,52753-63-6

bromobenzene

4-phenylalanine
92-67-1

4-phenylalanine

4-phenyldiphenylamine
32228-99-2

4-phenyldiphenylamine

Conditions
Conditions Yield
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; XPhos; In toluene; at 108 ℃; for 2h; Inert atmosphere;
86%
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; XPhos; In toluene; at 108 ℃; for 2h; Inert atmosphere;
86%
With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate; In toluene; at 80 ℃;
75%
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; XPhos; In toluene; for 1h; Inert atmosphere; Reflux;
75%
With tri-tert-butyl phosphine; palladium diacetate; sodium t-butanolate; In toluene; at 110 ℃; Inert atmosphere;
73%
With tris-(dibenzylideneacetone)dipalladium(0); tri-tert-butyl phosphine; sodium t-butanolate; In toluene; for 5h; Inert atmosphere; Reflux;
65%
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; tri tert-butylphosphoniumtetrafluoroborate; In toluene; at 100 ℃; for 7h; Inert atmosphere;
65%
With potassium phosphate; XPhos; tris-(dibenzylideneacetone)dipalladium(0); In toluene; for 20h; Heating;
aniline
62-53-3

aniline

4'-biphenyl chloride
2051-62-9,80333-62-6

4'-biphenyl chloride

4-phenyldiphenylamine
32228-99-2

4-phenyldiphenylamine

Conditions
Conditions Yield
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; XPhos; In toluene; at 70 ℃; for 1h; Inert atmosphere;
89.3%
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; XPhos; In toluene; at 65 - 75 ℃; for 1h; Inert atmosphere;
86.9%
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; XPhos; In toluene; at 20 - 70 ℃; for 1h; Inert atmosphere;
86.9%
aniline; 4'-biphenyl chloride; With palladium diacetate; sodium sulfate; sodium t-butanolate; XPhos; for 1h; Milling;
In water; ethyl acetate; for 0.0333333h; Milling;
62%
With [tert-butyloxy]bis(N,N-diisopropylamino)phosphane; bis(dibenzylideneacetone)-palladium(0); sodium t-butanolate; In toluene; at 105 ℃; for 24h; Inert atmosphere; Schlenk technique;

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