Uses
ChemicalBook > CAS DataBase List > 1,2,3-Trifluoro-4-nitrobenzene

1,2,3-Trifluoro-4-nitrobenzene

Uses
Product Name
1,2,3-Trifluoro-4-nitrobenzene
CAS No.
771-69-7
Chemical Name
1,2,3-Trifluoro-4-nitrobenzene
Synonyms
2,3,4-TRIFLUORONITROBENZENE;1,2,3-Trifluoro-4-ni;4-chloro-2-fluroaniline;4-Trifluoronitrobenzene;2,3,4-Trifluornitrobenzene;3,4,5 TRIFLUORONITROBENZEN;2,3,4-TRIFLUORONITROBRNZENE;1,2,3-Trifluor-4-nitrobenzol;2,3-Trifluoro-4-nitrobenzene;1-nitro-2,3,4-trifluorobenzene
CBNumber
CB7155826
Molecular Formula
C6H2F3NO2
Formula Weight
177.08
MOL File
771-69-7.mol
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1,2,3-Trifluoro-4-nitrobenzene Property

Boiling point:
92 °C/20 mmHg (lit.)
Density 
1.541 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.492(lit.)
Flash point:
200 °F
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Light yellow to Yellow to Orange
Specific Gravity
1.541
BRN 
2449746
InChI
InChI=1S/C6H2F3NO2/c7-3-1-2-4(10(11)12)6(9)5(3)8/h1-2H
InChIKey
ARCACZWMYGILNI-UHFFFAOYSA-N
SMILES
C1(F)=CC=C([N+]([O-])=O)C(F)=C1F
CAS DataBase Reference
771-69-7(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn,Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37/39-24/25
RIDADR 
UN2810
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
6.1
PackingGroup 
III
HS Code 
29042090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
338362
Product name
2,3,4-Trifluoronitrobenzene
Purity
99%
Packaging
25g
Price
$29
Updated
2023/06/20
TCI Chemical
Product number
T1539
Product name
2,3,4-Trifluoronitrobenzene
Purity
>98.0%(GC)
Packaging
5g
Price
$31
Updated
2025/07/31
TCI Chemical
Product number
T1539
Product name
2,3,4-Trifluoronitrobenzene
Purity
>98.0%(GC)
Packaging
25g
Price
$79
Updated
2025/07/31
TRC
Product number
T896260
Product name
2,3,4-Trifluoronitrobenzene
Packaging
5g
Price
$45
Updated
2021/12/16
TRC
Product number
T896260
Product name
2,3,4-Trifluoronitrobenzene
Packaging
10g
Price
$60
Updated
2021/12/16
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1,2,3-Trifluoro-4-nitrobenzene Chemical Properties,Usage,Production

Uses

2,3,4-Trifluoronitrobenzene is a useful research chemical.

Chemical Properties

clear yellow liquid after melting

Uses

2,3,4-Trifluoronitrobenzene was employed as starting reagent in the synthesis of ofloxacin. It was also used in the synthesis of the third generation quinolones antibacterial drugs.

General Description

2,3,4-Trifluoronitrobenzene is a fluoronitrobenzene and its biotransformation under methanogenic conditions has been studied by semicontinuous and batch tests. 2,3,4-Trifluoronitrobenzene is an important pharmaceutical intermediate.

Synthesis

17700-09-3

771-69-7

General procedure for the synthesis of 2,3,4-trifluoronitrobenzene from 2,3,4-trichloronitrobenzene: (2) 240 g of DMSO and 120 g of 2,3,4-trichloronitrobenzene were added to an anhydrous reaction flask with stirring turned on, and the temperature was raised to 75-80 °C under reduced pressure with continuous stirring for 2 hours. Subsequently, 76.8 g of KF and 12 g of TBAB were added to the reaction system and dehydrated under reduced pressure at 75-80 °C for 2 h until no droplets of water fell from the distillation head. (3) The reaction system was slowly warmed up to 180 °C to start the reaction. The reaction process was monitored by gas chromatography (GC), and the reaction was completed when the content of both 2-fluoro-3,4-dichloronitrobenzene and 2,3-dichloro-4-fluoronitrobenzene decreased to less than 0.2% after 10 h. The reaction was completed when the content of 2-fluoro-3,4-dichloronitrobenzene and 2,3-dichloro-4-fluoronitrobenzene dropped below 0.2%. The reaction mixture was cooled to 70-75 °C, filtered, and the filtrate was vacuum distilled and reintroduced into the anhydrous reaction unit. 46 g of KF and 12 g of TBAF were added and dehydrated under reduced pressure at 75-80 °C for 2 h until no water droplets appeared in the distillation head. The reaction temperature was set to 120 °C and ultrasonic power to 20 kHz and the reaction was continued. The reaction was monitored by GC and completed after 2 hours. The reaction mixture was cooled to 70-75°C and filtered and the filtrate was distilled to separate DMSO from the product. The final yield of 2,3,4-trifluoronitrobenzene was 99.7%.

References

[1] Patent: CN107325001, 2017, A. Location in patent: Paragraph 0028-0029; 0031-0034; 0036-0039; 0041-0044; 0046

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View Lastest Price from 1,2,3-Trifluoro-4-nitrobenzene manufacturers

.GZ HONESTCHEM CO.,LTD
Product
1,2,3-Trifluoro-4-nitrobenzene 771-69-7
Price
US $1.00/g
Min. Order
300g
Purity
99.8%
Supply Ability
20 TONS
Release date
2025-11-04
Shaanxi Dideu New Materials Co. Ltd
Product
1,2,3-Trifluoro-4-nitrobenzene 771-69-7
Price
US $0.00/kg
Min. Order
1kg
Purity
98%
Supply Ability
1000kg
Release date
2025-09-28
Hebei Chuanghai Biotechnology Co., Ltd
Product
1,2,3-Trifluoro-4-nitrobenzene 771-69-7
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500000kg
Release date
2024-10-31

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