3-Fluoro-2-nitropyridine CAS#: 54231-35-5; ChemWhat Code: 4708

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product Name3-fuoro-2-nitropyridine
IUPAC Name3-fluoro-2-nitropyridine
Molecular Structure3-Fluoro-2-nitropyridine-CAS-54231-35-5
CAS Registry Number 54231-35-5
Synonyms3-fuoro-2-nitropyridine, 2-nitro-3-fluoropyridine, 3- fluoro-2-nitropyridine, 3-fluoro-2-nitro-pyridine, 3-fluoro-2-nitropyridine, 2-Nitro-3-fluorpyridin
Molecular FormulaC5H3FN2O2
Molecular Weight142.089
InChIInChI=1S/C5H3FN2O2/c6-4-2-1-3-7-5(4)8(9)10/h1-3H
InChI KeyIJVFHCSUEBAAOZ-UHFFFAOYSA-N
Canonical SMILESC1=CC(=C(N=C1)[N+](=O)[O-])F
Patent Information
Patent IDTitlePublication Date
US2013/29961Substituted Heterocyclic Aza Compounds2013
US2013/29962Substituted Heteroaromatic Pyrazole-Containing Carboxamide and Urea Compounds as Vanilloid Receptor Ligands 2013

Physical Data

AppearanceYellow crystal
Melting Point35℃
38-39 ℃
Water SolubilitySlightly soluble in water
Flash Point>70℃

Spectra

Description (NMR Spectroscopy)Nucleus (NMR Spectroscopy)Solvents (NMR Spectroscopy)
Chemical shifts1HCDCl3
3-Fluoro-2-nitropyridine CAS#: 54231-35-5 UPLC3-Fluoro-2-nitropyridine CAS#: 54231-35-5 UPLC
3-Fluoro-2-nitropyridine CAS#: 54231-35-5 GC3-Fluoro-2-nitropyridine CAS#: 54231-35-5 GC

Route of Synthesis (ROS)

Route of Synthesis of 3-Fluoro-2-nitropyridine CAS 54231-35-5
ConditionsYield
Multi-step reaction with 2 steps
1: 87 percent / NaNO2, HBF4 (34percent) / H2O / 0.5 h / -8 – -2 °C
2: 115 – 120 °C
Stage #1: 3-amino-2-nitropyridine With tetrafluoroboric acid; sodium nitrite In water at -8 – -2℃ for 0.5h
Stage #2: at 120℃
Stage #3: With sodium hydrogencarbonate In water

Experimental Procedure
Step (i): Synthesis Of 3-fluoro-2-nitropyridineA solution of sodium nitrite (20 g, 288 mmol) in water (40 mL) was added dropwiseto a stirred mixture of2-nitropyridine-3-amine (40 g, 288 mmol) in 34percent fluoroboric acid(140 mL). During addition the temperature was maintained between -8 C to -2 DEG C. After0.5 h, the suspension was filtered and the solid washed with 34percent fkioroboric acid (35 mL),ether (80 mL) and dried at room temperature under high vacuurn for 12 h to give 52 g of an orange brown soud of the fluoroborate salt. The dry solid was decomposed by heating to 120 DEG C. Afler decomposition the remaining oil was treated with a solution of 10percent sodium hydrogenocarbonate (80mL) and the mixture was extracted with dichloromethane. The combined extracts were dried over sodium sulfate, filtered and the solvent removed overunder reduced pressure to yield the title compound as a pale yellow solid.
With tetrafluoroboric acid In toluene at 120℃ Inert atmosphere

Safety and Hazards

Pictogram(s)corrosionexclamation-mark
SignalDanger
GHS Hazard StatementsH302: Harmful if swallowed [Warning Acute toxicity, oral]
H314: Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
H315: Causes skin irritation [Warning Skin corrosion/irritation]
H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]
H335: May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Information may vary between notifications depending on impurities, additives, and other factors. 
Precautionary Statement CodesP260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501
(The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNot dangerous goods
Under the room temperature and away from light
HS Code294200
StorageStore at below 25°C for long time, in container tightly sealed; Protect from light
Shelf Life2 years
Market PriceUSD 2840/kg

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