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2-Fluoro-5-nitroaniline

CAS No.
369-36-8
Chemical Name:
2-Fluoro-5-nitroaniline
Synonyms
2-Fluoro-5-nitrobenzenamine;uoro-5-nitroaniL;Fluoronitroaniline1;2-Fluoro-5-nitroanil;5-Nitro-2-fluoroaniline;2-FLUORO-5-NITROANILINE;6-fluoro-3-nitroaniline;Aniline, 2-fluoro-5-nitro-;2-Fluoro-5-nitroaniline98%;2-Fluoro-5-nitroaniline>
CBNumber:
CB9226014
Molecular Formula:
C6H5FN2O2
Molecular Weight:
156.11
MDL Number:
MFCD00007652
MOL File:
369-36-8.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 04:18:46

2-Fluoro-5-nitroaniline Properties

Melting point 97-100 °C (lit.)
Boiling point 295.5±20.0 °C(Predicted)
Density 1.3822 (estimate)
Flash point 196 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Crystalline Powder
pka 1.13±0.10(Predicted)
color Ochre-yellow to light brown
Water Solubility Slightly soluble
BRN 2803491
InChI InChI=1S/C6H5FN2O2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H,8H2
InChIKey KJVBJICWGQIMOZ-UHFFFAOYSA-N
SMILES C1(N)=CC([N+]([O-])=O)=CC=C1F
CAS DataBase Reference 369-36-8(CAS DataBase Reference)
NIST Chemistry Reference 2-Fluoro-5-nitroaniline(369-36-8)
EPA Substance Registry System Benzenamine, 2-fluoro-5-nitro- (369-36-8)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Exclamation Mark (GHS07)
GHS02,GHS07
Signal word  Danger
Hazard statements  H228-H315-H319-H335
Precautionary statements  P210-P302+P352-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  F,Xi
Risk Statements  11-36/37/38
Safety Statements  16-26-36
RIDADR  UN 1325 4.1/PG 2
WGK Germany  3
Hazard Note  Irritant
HazardClass  6.1(b)
PackingGroup  III
HS Code  29214210
Storage Class 4.1B - Flammable solid hazardous materials
Hazard Classifications Eye Irrit. 2
Flam. Sol. 1
Skin Irrit. 2
STOT SE 3
Limited Quantities 1.0 Kg (2.2 lbs)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
2 0

2-Fluoro-5-nitroaniline price More Price(63)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 155853 2-Fluoro-5-nitroaniline 98% 369-36-8 25g $89.7 2026-04-30 Buy
Sigma-Aldrich 155853 2-Fluoro-5-nitroaniline 98% 369-36-8 100g $281 2023-06-20 Buy
TCI Chemical F0267 2-Fluoro-5-nitroaniline >99.0%(GC) 369-36-8 25g $65 2026-04-30 Buy
Usbiological 276011 2-Fluoro-5-nitroaniline Asreported 369-36-8 50g $382 2026-06-03 Buy
Usbiological 276011 2-Fluoro-5-nitroaniline Asreported 369-36-8 100g $542 2026-06-03 Buy
Product number Packaging Price Buy
155853 25g $89.7 Buy
155853 100g $281 Buy
F0267 25g $65 Buy
276011 50g $382 Buy
276011 100g $542 Buy

2-Fluoro-5-nitroaniline Chemical Properties, Uses, Production

Chemical Properties

ochre-yellow to light brown crystalline powder

Uses

It is employed as pharmaceutical intermediate.

Synthesis Reference(s)

Tetrahedron Letters, 31, p. 6141, 1990 DOI: 10.1016/S0040-4039(00)97008-4

Synthesis

2,4-Dinitrofluorobenzene

70-34-8

2-Fluoro-5-nitroaniline

369-36-8

The general procedure for the synthesis of 2-fluoro-5-nitroaniline from 2,4-dinitrofluorobenzene is as follows: 18.61 g (0.10 mol) of 2,4-dinitrofluorobenzene, 0.5 g of 5% palladium-carbon catalyst, 100 mL of glacial acetic acid, and 100 mL of anhydrous ethanol were added to a 500 mL Parr hydrogenation unit. The device was equipped with a thermocouple and a cooling jacket. During the reaction, the temperature of the reaction mixture was maintained at 20-25°C, the hydrogen pressure was maintained at 370 psi, and the reaction time was 2.5 hours. Upon completion of the reaction, the reaction mixture was poured into 400 mL of water. It was extracted twice with 200 mL of dichloromethane, the organic phases were combined and dried over anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure and the resulting residue was filtered through a silica gel pad and eluted with dichloromethane. The eluate was concentrated again under reduced pressure and the residue was further purified by column chromatography using dichloromethane:heptane (80:20, v/v) as eluent. Finally, the solvent was evaporated under reduced pressure to give 2.75 g of 2-fluoro-5-nitroaniline in 17.6% yield.

References

[1] Patent: US5105012, 1992, A
[2] Recueil des Travaux Chimiques des Pays-Bas, 1916, vol. 35, p. 142
[3] Chem. Zentralbl., 1913, vol. 84, # II, p. 760

Global Suppliers ( 298)
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View Latest Price from 2-Fluoro-5-nitroaniline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Fluoro-5-nitroaniline pictures 2026-09-02 2-Fluoro-5-nitroaniline
369-36-8
$8.00 1KG 99% Henan Fengda Chemical Co., Ltd
2-Fluoro-5-nitroaniline pictures 2026-08-07 2-Fluoro-5-nitroaniline
369-36-8
$1.00-4.00 1KG 99% 200000KG Shaanxi Dideu Medichem Co. Ltd
2-Fluoro-5-nitroaniline pictures 2026-06-30 2-Fluoro-5-nitroaniline
369-36-8
1KG 98.0% 10000KGS Shaanxi Dideu New Materials Co. Ltd
1-Amino-2-fluoro-5-nitrobenzene Aniline, 2-fluoro-5-nitro- Benzenamine, 2-fluoro-5-nitro- 2-FLUORO-5-NITROANILINE F03860 2-Fluoro-5-nitroaniline Fluoronitroaniline1 2-Fluoro-5-nitroaniline 96% 2-Fluoro-5-nitroaniline98% 2-Fluoro-5-nitrobenzenamine 5-Nitro-2-fluoroaniline 2-Fluoro-5-nitroaniline, 98% 25GR 2-Fluoro-5-nitroaniline, 98% 5GR 2-Fluoro-5-nitroaniline, 97+% 2-Fluoro-5-nitroanil 3-Amino-4-fluoronitrobenzene 6-fluoro-3-nitroaniline 2-Fluoro-5-nitroaniline> uoro-5-nitroaniL 369-36-8 (2-FLUORO-5-NITROANILINE ) 2-Fluoro-5-nitroaniline ISO 9001:2015 REACH 369-36-8 FC6H3NO2NH2 Building Blocks Amines C2 to C6 Nitrogen Compounds Organic Building Blocks Aniline series Amines C2 to C6 Nitrogen Compounds Anilines, Aromatic Amines and Nitro Compounds API intermediates