369-35-7

  • Product Name:2-Fluoro-4-nitroaniline
  • Molecular Formula:C6H5FN2O2
  • Purity:99%
  • Molecular Weight:156.116
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Product Details;

CasNo: 369-35-7

Molecular Formula: C6H5FN2O2

Appearance: WHITE TO TAN POWDER, CRYSTALS OR CRYSTALLINE POWDER AND/OR CHUNKS

factory and supplier 369-35-7 2-Fluoro-4-nitroaniline in stock

  • Molecular Formula:C6H5FN2O2
  • Molecular Weight:156.116
  • Appearance/Colour:WHITE TO TAN POWDER, CRYSTALS OR CRYSTALLINE POWDER AND/OR CHUNKS 
  • Vapor Pressure:0.000392mmHg at 25°C 
  • Melting Point:126-130°C 
  • Refractive Index:1.603 
  • Boiling Point:317.2 °C at 760 mmHg 
  • PKA:-0.45±0.10(Predicted) 
  • Flash Point:145.6 °C 
  • PSA:71.84000 
  • Density:1.448 g/cm3 
  • LogP:2.42050 

2-Fluoro-4-nitroaniline(Cas 369-35-7) Usage

Purification Methods

The aniline forms yellow crystals on recrystallisation from aqueous MeOH or EtOH. The acetyl derivative has m 203-204o (from EtOH). [Wepster & Verkade Recl Trav Chim, Pays Bas 68 86 1949, Beilstein 12 III 1647.]

InChI:InChI=1/C6H5FN2O2/c7-5-3-4(9(10)11)1-2-6(5)8/h1-3H,8H2

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369-35-7 Process route

N-(2-fluorophenyl)acetamide
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N-(2-fluorophenyl)acetamide

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2-fluoro-6-nitroaniline

2-fluoro-4-nitroaniline
369-35-7

2-fluoro-4-nitroaniline

Conditions
Conditions Yield
N-(2-fluorophenyl)acetamide; With sulfuric acid; nitric acid; In acetic acid; at 10 - 20 ℃; for 2.5h;
With sodium hydroxide; In ethanol; water; for 5h;
15.3%
67.5%
With hydrogenchloride; nitric acid; Multistep reaction; 1.) acetic anhydride-acetic acid, 0-5 deg C;
3-fluoro-1-nitrobenzene
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2-nitro-4-fluoroaniline
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2-nitro-4-fluoroaniline

2-fluoro-6-nitroaniline
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2-fluoro-6-nitroaniline

2-fluoro-4-nitroaniline
369-35-7

2-fluoro-4-nitroaniline

Conditions
Conditions Yield
With O-Methylhydroxylamin; potassium tert-butylate; copper(l) chloride; In N,N-dimethyl-formamide; for 1h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature;
With potassium tert-butylate; N,N,N-trimethylhydrazinium iodide; In dimethyl sulfoxide; Yield given. Yields of byproduct given; Ambient temperature;
With O-Methylhydroxylamin; potassium tert-butylate; copper(l) chloride; In N,N-dimethyl-formamide; at 20 ℃; Title compound not separated from byproducts;

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