ChemicalBook--->CAS DataBase List--->34667-88-4

34667-88-4

34667-88-4 Structure

34667-88-4 Structure
IdentificationMore
[Name]

2-FLUORO-4-NITROBENZONITRILE
[CAS]

34667-88-4
[Synonyms]

2-FLUORO-4-NITROBENZONITRILE
2-Fluoro-4-nitrobenzonitrile ,98%
[Molecular Formula]

C7H3FN2O2
[MDL Number]

MFCD04038715
[Molecular Weight]

166.11
[MOL File]

34667-88-4.mol
Chemical PropertiesBack Directory
[Melting point ]

0°C
[Boiling point ]

0°C
[density ]

1.41±0.1 g/cm3(Predicted)
[Fp ]

0°C
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Off-white to light yellow Solid
[Detection Methods]

HPLC,NMR
[CAS DataBase Reference]

34667-88-4(CAS DataBase Reference)
Safety DataBack Directory
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

3439
[HS Code ]

29269090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Ethyl acetate-->Diethyl ether-->Sulfuric acid-->Tetrahydrofuran-->Potassium carbonate-->Triethylamine-->Chromium(VI) oxide-->Trifluoroacetic anhydride-->Oxalyl chloride-->2-Fluoro-4-nitrotoluene-->2-Fluoro-4-nitrobenzoic acid-->2-Fluoro-4-nitrobenzoyl chloride-->2-Fluoro-4-nitro-benzamide-->2 4-Dinitrobenzonitrile 97-->1-Bromo-2,4-dinitrobenzene
[Preparation Products]

2,4-Difluorobenzonitrile-->4-Amino-2-fluorobenzonitrile
Hazard InformationBack Directory
[Chemical Properties]

Light yellow solid
[Synthesis]

2-Fluoro-4-nitro-benzamide

350-32-3

2-FLUORO-4-NITROBENZONITRILE

34667-88-4

General procedure for the synthesis of 2-fluoro-4-nitrobenzonitrile from 2-fluoro-4-nitrobenzamide: A mixture of 2-fluoro-4-nitrobenzamide (0.83 g, 4.6 mmol) and phosphorus pentoxide/hexamethyldisiloxane in 1,2-dichloroethane (20 mL) was heated and refluxed for 4 hr at 100 °C under nitrogen atmosphere. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently filtered through a silicone plug, washed first with hexane (200 mL) and then with 5% methanol/chloroform mixture (400 mL). The methanol/chloroform washings were combined and concentrated under reduced pressure to give 2-fluoro-4-nitrobenzonitrile (0.71 g, 95% yield) as a beige solid.1H NMR (DMSO-d6) data were as follows: δ 8.46 (dd, J = 9.5, 2.0 Hz, 1H), 8.37-8.22 (m, 2H).

[References]

[1] Journal of Heterocyclic Chemistry, 1997, vol. 34, # 4, p. 1163 - 1172
[2] Patent: US6344459, 2002, B1. Location in patent: Page column 70-71
[3] European Journal of Medicinal Chemistry, 2018, vol. 143, p. 1325 - 1344
[4] Journal of Medicinal Chemistry, 2001, vol. 44, # 23, p. 3856 - 3871
Spectrum DetailBack Directory
[Spectrum Detail]

2-FLUORO-4-NITROBENZONITRILE(34667-88-4)1HNMR
2-FLUORO-4-NITROBENZONITRILE(34667-88-4)19FNMR
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