
3862-73-5
- Product Name:2,3,4-Trifluoroaniline
- Molecular Formula:C6H4F3N
- Purity:99%
- Molecular Weight:147.1
Product Details;
CasNo: 3862-73-5
Molecular Formula: C6H4F3N
Appearance: Pale yellow liquid
Reliable Quality Chinese Manufacturer Supply 2,3,4-Trifluoroaniline 3862-73-5 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
Chemical Properties |
CLEAR PURPLE TO BROWN LIQUID |
Uses |
2,3,4-Trifluoroaniline was used in preparation of diethyl 2-(2,3,4-trifluoro)-phenylaminomethylene malonate. |
General Description |
Study on synthesis of 2,3,4-trifluoroaniline was reported. |
Safety Profile |
Moderately toxic by ingestion. Askin and eye irritant. Combustible liquid. When heated todecomposition it emits toxic fumes of NOx and F??. |
Consumer Uses |
ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment. |
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
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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
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Paragraph 0018-0033, (2019/01/06)
The invention provides a method for prod...
3862-73-5 Process route
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- 771-69-7
2,3,4-trifluoronitrobenzene

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- 369-34-6
3,4-difluoronitrobenzene

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- 6921-22-8
1,2-difluoro-3-nitrobenzene

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- 3862-73-5
2,3,4-trifluoroaniline
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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- 367-25-9,76563-56-9
2,4-difluorophenylamine

-
- 367-34-0
2,4,5-trifluoroaniline

-
- 3862-73-5
2,3,4-trifluoroaniline
Conditions | Yield |
---|---|
With trifluorormethanesulfonic acid; fluorine; at 20 ℃; Title compound not separated from byproducts;
|
3862-73-5 Upstream products
-
771-69-7
2,3,4-trifluoronitrobenzene
-
367-25-9
2,4-difluorophenylamine
-
62-53-3
aniline
-
371-40-4
4-fluoroaniline
3862-73-5 Downstream products
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119474-39-4
triethylammonium N-(2,3,4-trifluorophenyl)dithiocarbamate
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100501-60-8
diethyl 2-((2,3,4-trifluorophenylamino)methylene)malonate
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365-29-7
N-(2,3,4-trifluorophenyl)acetamide
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134364-69-5
2.3-difluoroanisole
Relevant Products
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1,2,3-Trifluoro-4-nitrobenzene
CAS:771-69-7
-
3,5-Difluoroaniline
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2,3-Difluoro-5-chloropyridin
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