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5-FLUORO-2-NITROBENZAMIDE

Product Name
5-FLUORO-2-NITROBENZAMIDE
CAS No.
77206-97-4
Chemical Name
5-FLUORO-2-NITROBENZAMIDE
Synonyms
5-FLUORO-2-NITROBENZAMIDE;Benzamide, 5-fluoro-2-nitro-;5-fluoro-2-nitrobenzamide5-fluoro-2-nitrobenzamide
CBNumber
CB92466443
Molecular Formula
C7H5FN2O3
Formula Weight
184.12
MOL File
77206-97-4.mol
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5-FLUORO-2-NITROBENZAMIDE Property

storage temp. 
Sealed in dry,Room Temperature
Appearance
Off-white to light yellow Solid
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Safety

HS Code 
2924297099
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
F597593
Product name
5-Fluoro-2-nitrobenzamide
Packaging
100mg
Price
$45
Updated
2021/12/16
TRC
Product number
F597593
Product name
5-Fluoro-2-nitrobenzamide
Packaging
250mg
Price
$85
Updated
2021/12/16
TRC
Product number
F597593
Product name
5-Fluoro-2-nitrobenzamide
Packaging
500mg
Price
$125
Updated
2021/12/16
AK Scientific
Product number
V7707
Product name
5-Fluoro-2-nitrobenzamide
Packaging
1g
Price
$81
Updated
2021/12/16
Ambeed
Product number
A300132
Product name
5-Fluoro-2-nitrobenzamide
Purity
97%
Packaging
250mg
Price
$18
Updated
2021/12/16
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5-FLUORO-2-NITROBENZAMIDE Chemical Properties,Usage,Production

Synthesis

394-02-5

77206-97-4

General procedure for the synthesis of 5-fluoro-2-nitrobenzamide from 5-fluoro-2-nitrobenzoyl chloride: anhydrous tetrahydrofuran (THF, 3 mL) solution of oxalyl chloride (1.83 g, 14.4 mmol) was added slowly and dropwise at 0 °C and under nitrogen protection to commercially available 5-fluoro-2-nitrobenzoic acid (1.78 g, 9.62 mmol) and N,N-dimethylformamide ( DMF, 40 mg) in a solution of anhydrous THF (10 mL). After the reaction mixture was stirred at room temperature for 1.5 h, the solvent was removed by vacuum evaporation to give 5-fluoro-2-nitrobenzoyl chloride (2.13 g) as a yellow oil. Subsequently, a solution of anhydrous THF (9 mL) of 5-fluoro-2-nitrobenzoyl chloride (1.53 g) was slowly added to pre-cooled 35% ammonia (30 mL) at room temperature. The reaction mixture was stirred for 45 min and extracted by adding dichloromethane (50 mL). The organic layer was separated and the aqueous layer was extracted once more with dichloromethane (50 mL). The combined organic phases were washed with saturated aqueous ammonium chloride solution (1 x 50 mL), dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated to dryness in vacuum to afford 5-fluoro-2-nitrobenzamide (1.04 g, 75% yield, liquid chromatographic purity >95%). Mass spectrometry analysis: [M+H]+=185.

References

[1] Patent: US2010/280268, 2010, A1. Location in patent: Page/Page column 46-47
[2] Patent: WO2008/74749, 2008, A1. Location in patent: Page/Page column 58
[3] Patent: WO2006/34491, 2006, A2. Location in patent: Page/Page column 43
[4] European Journal of Medicinal Chemistry, 2011, vol. 46, # 7, p. 2709 - 2721
[5] Patent: WO2014/143960, 2014, A1. Location in patent: Page/Page column 39-40

5-FLUORO-2-NITROBENZAMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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5-FLUORO-2-NITROBENZAMIDE Suppliers

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77206-97-4, 5-FLUORO-2-NITROBENZAMIDERelated Search:


  • 5-FLUORO-2-NITROBENZAMIDE
  • Benzamide, 5-fluoro-2-nitro-
  • 5-fluoro-2-nitrobenzamide5-fluoro-2-nitrobenzamide
  • 77206-97-4