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4-Methoxy-N-(4-methoxyphenyl)

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Products Intro: Product Name:4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline
CAS:20440-94-2
Purity:98% HPLC Package:500g;1kg;5kg;10kg;25kg
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Products Intro: Product Name:4,4'-Dimethoxytriphenylamine
CAS:20440-94-2
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Products Intro: Product Name:4,4-Dimethoxy-triphenylamine
CAS:20440-94-2
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Products Intro: Product Name:4-Methoxy-N-(4-methoxyphenyl)-N-phenylbenzenamine
CAS:20440-94-2
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Products Intro: Product Name:4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline
CAS:20440-94-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-30738

4-Methoxy-N-(4-methoxyphenyl) manufacturers

4-Methoxy-N-(4-methoxyphenyl) Basic information
Product Name:4-Methoxy-N-(4-methoxyphenyl)
Synonyms:4,4'-Dimethoxytriphenylamine;4-Methoxy-N-(4-methoxyphenyl)-N-phenylbenzenamine;Benzenamine, 4-methoxy-N-(4-methoxyphenyl)-N-phenyl-;4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline, 95+%;4,4'-Dimethoxy triphenylamine;4-Methoxy-N-(4-Methoxyphenyl)-N-phenylaniline
CAS:20440-94-2
MF:C20H19NO2
MW:305.37
EINECS:
Product Categories:
Mol File:20440-94-2.mol
4-Methoxy-N-(4-methoxyphenyl) Structure
4-Methoxy-N-(4-methoxyphenyl) Chemical Properties
Melting point 103 °C
Boiling point 453.4±30.0 °C(Predicted)
density 1.136
storage temp. Sealed in dry,Room Temperature
pka-1.74±0.50(Predicted)
AppearanceOff-white to light yellow Solid
InChIInChI=1S/C20H19NO2/c1-22-19-12-8-17(9-13-19)21(16-6-4-3-5-7-16)18-10-14-20(23-2)15-11-18/h3-15H,1-2H3
InChIKeyZJPTYHDCQPDNBH-UHFFFAOYSA-N
SMILESC1(N(C2=CC=C(OC)C=C2)C2=CC=CC=C2)=CC=C(OC)C=C1
Safety Information
MSDS Information
4-Methoxy-N-(4-methoxyphenyl) Usage And Synthesis
Uses4-Methoxy-N-(4-methoxyphenyl) (also known as 4,4'-dimethoxytriphenylamine) is a synthetic material intermediate, which can be used to prepare hole transport materials (HTMs) for perovskite solar cells (PSCs).
Synthesis
4-Bromoanisole

104-92-7

Aniline

62-53-3

4-Methoxy-N-(4-methoxyphenyl)-N-phenylbenzenamine

20440-94-2

To a 1L three-neck flask were added 18.63 g (0.2 mol) of aniline, 78.55 g (0.42 mol) of 4-bromoanisole, 56.10 g (0.5 mol) of potassium tert-butanol and 465.7 g of toluene. Subsequently, 3.66 g (4.0 x 10^-3 mol) of Pd2(dba)3 and 2.32 g (8.0 x 10^-3 mol) of (t-Bu)3PH-BF4 were added as catalysts. The reaction mixture was heated to 100~108°C for 4 hours. After completion of the reaction, the reaction solution was filtered and the filtrate was washed with 200 g of water and dried with anhydrous sodium sulfate. Purification by silica gel column chromatography using toluene as eluent gave a brown viscous liquid. The above crude product was recrystallized with toluene and ethanol (mass ratio 1:2) to afford 51.0 g of 4,4'-dimethoxytriphenylamine in yellow powder form in 83.5% yield.

References[1] European Journal of Organic Chemistry, 2016, vol. 2016, # 10, p. 1908 - 1914
[2] Chemical Communications, 2018, vol. 54, # 6, p. 642 - 645
[3] Journal of Materials Chemistry A, 2018, vol. 6, # 17, p. 7950 - 7958
[4] Patent: CN106565507, 2017, A. Location in patent: Paragraph 0112; 0113; 0114; 0115
[5] Chemistry - A European Journal, 2015, vol. 21, # 46, p. 16673 - 16678
4-Methoxy-N-(4-methoxyphenyl) Preparation Products And Raw materials
Raw materials4-Bromoanisole-->4-Iodoanisole-->Aniline-->Tris(dibenzylideneacetone)dipalladium-->Tri-tert-butylphosphine tetrafluoroborate-->Potassium tert-butoxide-->Toluene
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