ChemicalBook--->CAS DataBase List--->157662-77-6

157662-77-6

157662-77-6 Structure

157662-77-6 Structure
IdentificationBack Directory
[Name]

(4-FLUORO-3-NITROPHENYL)ACETONITRILE
[CAS]

157662-77-6
[Synonyms]

(4-FLUORO-3-NITROPHENYL)ACETONITRILE
Benzeneacetonitrile, 4-fluoro-3-nitro-
2-(4-FLUORO-3-NITROPHENYL)ACETONITRILE
1,3-Dioxane-4,6-dione,2,2-dimethyl-8-phenyl-
[Molecular Formula]

C8H5FN2O2
[MDL Number]

MFCD09909410
[MOL File]

157662-77-6.mol
[Molecular Weight]

180.14
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[HS Code ]

2926907090
Hazard InformationBack Directory
[Application]

(4-Fluoro-3-Nitrophenyl)Acetonitrile is a useful research chemical compound.
[Synthesis]

TETRAETHYLAMMONIUM CYANIDE

13435-20-6

4-Fluoro-3-nitrobenzyl bromide

15017-52-4

(4-FLUORO-3-NITROPHENYL)ACETONITRILE

157662-77-6

34A: Synthesis of 2-(4-fluoro-3-nitrophenyl)acetonitrile To a solution of 4-(bromomethyl)-1-fluoro-2-nitrobenzene (1 g, 4.27 mmol) in acetonitrile (5 mL) was added tetraethylammonium cyanide (0.801 g, 5.13 mmol). The reaction mixture was stirred at room temperature for 4 h. The reaction solution was dark green in color. After completion of the reaction, the solvent was removed by rotary evaporator under reduced pressure. The crude product was purified by fast column chromatography to afford 34A (light yellow oil, 617 mg, 3.43 mmol, 80% yield).LC-MS analysis: calculated value of C8H5F2O2 was 180.03, no parent ion was observed, retention time (Tr) = 0.74 min (Method B).

[References]

[1] Patent: WO2014/150646, 2014, A1. Location in patent: Page/Page column 76; 77
[2] Journal of the Chemical Society - Series Chemical Communications, 1994, # 4, p. 439 - 440
Spectrum DetailBack Directory
[Spectrum Detail]

(4-FLUORO-3-NITROPHENYL)ACETONITRILE(157662-77-6)1HNMR
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