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2,3,4,6-Tetrafluoronitrobenzene

CAS No.
314-41-0
Chemical Name:
2,3,4,6-Tetrafluoronitrobenzene
Synonyms
1,2,3,5-Tetrafluoro-4-nitrobenzene;2,3,4,6-TetrafL;2,3,4,6-TETRAFLUORON;5-fluro-2-methylaniline;5-tetrafluoro-4-nitrobenzene;1,2,4,6-Tetrafluoronitrobenzene;2,3,4,6-Tetrafluoronitrobenzene;2-Nitro-1,3,4,5-tetrafluorobenzene;1-Nitro-2,3,4,6-tetrafluorobenzene;2,3,4,6-Tetrafluoronitrobenzene98%
CBNumber:
CB5351352
Molecular Formula:
C6HF4NO2
Molecular Weight:
195.07
MDL Number:
MFCD00011687
MOL File:
314-41-0.mol
MSDS File:
SDS
Last updated:2026-09-12 18:53:30

2,3,4,6-Tetrafluoronitrobenzene Properties

Melting point -5
Boiling point 78-79°C 20mm
Density 1.511 g/mL at 25 °C (lit.)
refractive index n20/D 1.464(lit.)
Flash point 160 °F
storage temp. 2-8°C
form liquid
Specific Gravity 1.511
Appearance Colorless to light yellow Liquid
Stability Stable. Incompatible with strong oxidizing agents, strong bases. Combustible.
InChI 1S/C6HF4NO2/c7-2-1-3(8)6(11(12)13)5(10)4(2)9/h1H
InChIKey FDLCUAUNAWWSBX-UHFFFAOYSA-N
SMILES [O-][N+](=O)c1c(F)cc(F)c(F)c1F
CAS DataBase Reference 314-41-0(CAS DataBase Reference)
FDA UNII SU82FD6B27
EPA Substance Registry System Benzene, 1,2,3,5-tetrafluoro-4-nitro- (314-41-0)
UNSPSC Code 12352100

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36/37/39
WGK Germany  3
HazardClass  IRRITANT
HS Code  2904990090
Storage Class 10 - Combustible liquids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

2,3,4,6-Tetrafluoronitrobenzene price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FT97972 2,3,4,6-Tetrafluoronitrobenzene 314-41-0 10g $584.1 2026-06-04 Buy
Biosynth FT97972 2,3,4,6-Tetrafluoronitrobenzene 314-41-0 25g $778.75 2026-06-04 Buy
Biosynth FT97972 2,3,4,6-Tetrafluoronitrobenzene 314-41-0 50g $1038.5 2026-06-04 Buy
Biosynth FT97972 2,3,4,6-Tetrafluoronitrobenzene 314-41-0 100g $1622 2026-06-04 Buy
Apolloscientific PC6810 2,3,4,6-Tetrafluoronitrobenzene 97% 314-41-0 250mg $48 2026-06-04 Buy
Product number Packaging Price Buy
FT97972 10g $584.1 Buy
FT97972 25g $778.75 Buy
FT97972 50g $1038.5 Buy
FT97972 100g $1622 Buy
PC6810 250mg $48 Buy

2,3,4,6-Tetrafluoronitrobenzene Chemical Properties, Uses, Production

Chemical Properties

yellow liquid

Uses

Molluscicidal activity of 2,3,4,6-tetrafluoronitrobenzene against Biomphalaria glabrata has been investigated. Palladium-catalyzed cross-coupling reactions of 2,3,4,6-tetrafluoronitrobenzene with alkyne derivatives has been studied. Reaction of 2,3,4,6-tetrafluoronitrobenzene with 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene in the presence of water molecules in acetonitrile has been investigated.

General Description

Molluscicidal activity of 2,3,4,6-tetrafluoronitrobenzene against Biomphalaria glabrata has been investigated. Palladium-catalyzed cross-coupling reactions of 2,3,4,6-tetrafluoronitrobenzene with alkyne derivatives has been studied. Reaction of 2,3,4,6-tetrafluoronitrobenzene with 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene in the presence of water molecules in acetonitrile has been investigated.

Synthesis

1,2,3,5-Tetrafluorobenzene

2367-82-0

2,3,4,6-TETRAFLUORONITROBENZENE

314-41-0

For the large-scale synthesis of 1,2,3,5-tetrafluoro-4-nitrobenzene, a mixed solution of concentrated nitric acid (990 g) in concentrated sulfuric acid (973 mL) was first pre-cooled, and then the mixed solution was slowly added to a cold solution of 1,2,3,5-tetrafluorobenzene (973.1 g) dissolved in concentrated sulfuric acid (2,920 mL) at temperatures ranging from 0 °C to 10 °C, with the addition process being controlled to be completed within 1.5 The addition process was completed within 1.5 hours. After the addition was completed, the reaction temperature was maintained between 0 °C and 10 °C, and the yellow reaction solution was continued to be stirred for 1 hour until the analysis confirmed the completion of the reaction. Subsequently, the reaction solution was slowly poured into water (9730 g) that had been pre-cooled to below 25 °C, and dichloromethane (9730 mL) was added for extraction. After separation of the organic phase, it was washed twice with deionized water (10 L). The dichloromethane layer was concentrated to give a yellow oil. Finally, the oily substance was distilled under reduced pressure (2.5 mbar) at 70 °C to 75 °C to give a yellow oily product with 98% purity and 72.4% yield.

References

[1] Journal of Organic Chemistry, 1995, vol. 60, # 22, p. 7348 - 7350
[2] Patent: US2012/316149, 2012, A1. Location in patent: Page/Page column 11
[3] Patent: WO2012/168884, 2012, A1. Location in patent: Page/Page column 26; 27
[4] Russian Chemical Bulletin, 1998, vol. 47, # 5, p. 924 - 927
[5] Journal of the American Chemical Society, 1951, vol. 73, p. 153

2,3,4,6-Tetrafluoronitrobenzene Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 123)
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Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
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Huainan Kedi Chemical Factory 0554-2106669 sales1@kedichem.com China 4914 55
Benzene, 1,2,3,5-tetrafluoro-4-nitro- 2,3,4,6-TETRAFLUORONITROBENZENE, 97+% 2,3,4,6-TETRAFLUORON 1,2,4,6-Tetrafluoronitrobenzene 5-tetrafluoro-4-nitrobenzene 2-Nitro-1,3,4,5-tetrafluorobenzene 5-fluro-2-methylaniline 2,3,4,6-Tetrafluoronitrobenzene 98% 2,3,4,6-Tetrafluoronitrobenzene98% 1-Nitro-2,3,4,6-tetrafluorobenzene 2,3,4,6-TetrafL 2,3,4,6-TETRAFLUORONITROBENZENE ISO 9001:2015 REACH 1,2,3,5-Tetrafluoro-4-nitrobenzene 2,3,4,6-Tetrafluoronitrobenzene 314-41-0 C6HF4NO2 HC6F4NO2 Building Blocks Nitrogen Compounds Organic Building Blocks Nitro Compounds Benzene series Nitro Compounds Nitrogen Compounds Organic Building Blocks