341-58-2

  • Product Name:2,2'-Bis(Trifluoromethyl)Diaminobiphenyl
  • MF:C14H10F6N2
  • Purity:99%
  • Molecular Weight:320.237
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Product Details

Good factory supply good 2,2'-Bis(Trifluoromethyl)Diaminobiphenyl 341-58-2

  • Molecular Formula:C14H10F6N2
  • Molecular Weight:320.237
  • Appearance/Colour:white crystalline powder 
  • Melting Point:183 °C 
  • Boiling Point:376.9 °C at 760 mmHg 
  • PKA:3.23±0.10(Predicted) 
  • Flash Point:171.4 °C 
  • PSA:52.04000 
  • Density:1.415 g/cm3 
  • LogP:5.71800 

341-58-2 Relevant articles

Homocoupling of a Grignard Reagent toward the Synthesis of 2,2′-Bis(trifluoromethyl)-4,4′-diaminobiphenyl

Nakatani, Jiro,Nozoe, Tatsuhiro

supporting information, p. 2442 - 2446 (2021/11/13)

A new process for the synthesis of 2,2′-...

METHOD OF MANUFACTURING BIS(TRIFLUOROMEHTYL)DIAMINOBIPHENYL COMPOUND

-

Paragraph 0056-0089, (2021/09/21)

To exemplary embodiments of the present ...

Preparation method of 2,2'-bis (trifluoromethyl)-4,4'-diaminobiphenyl

-

Paragraph 0027; 0031-0033; 0037-0039; 0043-0045; 0049; ..., (2021/06/26)

The invention discloses a preparation me...

Preparation Method for 2,2'-Bis(Trifluoromethyl)-4,4'-Diaminobiphenyl

-

Paragraph 0026-0037, (2021/07/20)

The present invention relates to a metho...

341-58-2 Process route

2,2'-bis-(trifluoromethyl)-4,4'-dinitro-1,1'-biphenyl
641-98-5

2,2'-bis-(trifluoromethyl)-4,4'-dinitro-1,1'-biphenyl

2,2'-bis(trifluoromethyl)benzidine
341-58-2

2,2'-bis(trifluoromethyl)benzidine

Conditions
Conditions Yield
With ammonium formate; zinc; In methanol; at 50 ℃; Temperature; Concentration;
96.83%
With 5%-palladium/activated carbon; hydrogen; In water; isopropyl alcohol; at 50 - 60 ℃; for 4h; under 225.023 - 375.038 Torr; Solvent; Autoclave;
94%
With sodium hydrogen sulfide monohydrate; In methanol; for 15h; Solvent; Temperature; Reflux;
93%
With palladium 10% on activated carbon; hydrogen; In ethanol; at 80 ℃; under 15001.5 Torr; Pressure; Temperature; Catalytic behavior;
92%
With hydrogenchloride; tin;
With hydrogen; palladium on activated charcoal; In toluene; at 60 ℃; for 6h; under 7500.75 Torr; Autoclave;
1,2-bis(3-(trifluoromethyl)phenyl)hydrazine
351-19-9

1,2-bis(3-(trifluoromethyl)phenyl)hydrazine

2,2'-bis(trifluoromethyl)benzidine
341-58-2

2,2'-bis(trifluoromethyl)benzidine

Conditions
Conditions Yield
With sulfuric acid; In water; toluene; for 5h; Product distribution / selectivity;
95.1%
With hydrogenchloride; In water; toluene; at 25 ℃; for 3h; Product distribution / selectivity;
95%
With hydrogenchloride; In methanol; water; at 0 ℃; for 6h; Temperature; Reagent/catalyst; Inert atmosphere;
61.2%
With sulfuric acid; In water; at -5 - 75 ℃; for 2h; under 2280.15 - 3800.26 Torr; Temperature; Inert atmosphere;
60%
With sulfuric acid; In water; at 20 ℃; for 2h; Temperature; Inert atmosphere;
29.8%
With sulfuric acid; In ethanol; water; at 0 ℃; for 12h; Product distribution / selectivity;
9.5%
With hydrogenchloride; In ethanol; water; at 0 ℃; for 24h; Product distribution / selectivity;
2.4%
With sulfuric acid; In water; toluene; for 5h; Product distribution / selectivity;
31.8 - 95.1 %Chromat.
With hydrogenchloride; In water; toluene; at 25 ℃; for 3h; Product distribution / selectivity;
With hydrogenchloride; In ethanol; water; at 0 ℃; for 24h; Product distribution / selectivity;
2.4 %Chromat.
With sulfuric acid; In ethanol; water; at 20 ℃; for 12h; Product distribution / selectivity;
9.5 %Chromat.
With sulfuric acid; at 20 ℃; for 4.5h;
55.8 g

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341-58-2 Downstream products

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