3862-73-5

  • Product Name:2,3,4-Trifluorobenzenamine
  • Molecular Formula:C6H4F3N
  • Purity:99%
  • Molecular Weight:147.1
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Product Details;

CasNo: 3862-73-5

Molecular Formula: C6H4F3N

Appearance: Pale yellow liquid

factory and supplier 3862-73-5 2,3,4-Trifluorobenzenamine in stock

  • Molecular Formula:C6H4F3N
  • Molecular Weight:147.1
  • Appearance/Colour:Pale yellow liquid 
  • Vapor Pressure:0.00696mmHg at 25°C 
  • Melting Point:14-15°C 
  • Refractive Index:n20/D 1.486(lit.)  
  • Boiling Point:173.8 °C at 760 mmHg 
  • PKA:2.25±0.10(Predicted) 
  • Flash Point:71.8 °C 
  • PSA:26.02000 
  • Density:1.409 g/cm3 
  • LogP:2.26730 

2,3,4-Trifluorobenzenamine(Cas 3862-73-5) Usage

Safety Profile

Moderately toxic by ingestion. Askin and eye irritant. Combustible liquid. When heated todecomposition it emits toxic fumes of NOx and F??.

General Description

Study on synthesis of 2,3,4-trifluoroaniline was reported.

InChI:InChI=1/C7H5F3N2O/c8-7(9,10)5-2-1-4(3-12-5)6(11)13/h1-3H,(H2,11,13)

3862-73-5 Relevant articles

Pd-CATALYZED AMINATION OF FLUORINATED ARYL CHLORIDES

-

Page/Page column 12; 13, (2021/10/15)

The presently claimed invention relates ...

Preparation method of 3, 4, 5-trifluorobromobenzene

-

, (2020/12/14)

The invention relates to a preparation m...

Highly selective hydrogenation of halogenated nitroarenes over Ru/CN nanocomposites by: In situ pyrolysis

Yue, Shengnan,Wang, Xueguang,Li, Shaoting,Sheng, Yao,Zou, Xiujing,Lu, Xionggang,Zhang, Chunlei

, p. 11861 - 11869 (2020/07/28)

A highly chemoselective and recyclable r...

Method for producing 2,3,4-trifluoroaniline by adopting solvent-free catalytic hydrogenation

-

Paragraph 0018-0033, (2019/01/06)

The invention provides a method for prod...

3862-73-5 Process route

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Conditions
Conditions Yield
With Dimethylphenylsilane; o-phenylenebis(diphenylphosphine); potassium tert-butylate; copper(l) chloride; In tetrahydrofuran; for 12h; Overall yield = 95 %Spectr.; regioselective reaction; Inert atmosphere; Reflux;
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Conditions
Conditions Yield
With trifluorormethanesulfonic acid; fluorine; at 20 ℃; Title compound not separated from byproducts;

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