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2-FLUORO-6-NITRO-PHENYLAMINE

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2-FLUORO-6-NITRO-PHENYLAMINE Basic information

Product Name:
2-FLUORO-6-NITRO-PHENYLAMINE
Synonyms:
  • 2-FLUORO-6-NITROANILINE
  • 2-FLUORO-6-NITRO-PHENYLAMINE
  • 2-Fluoro-6-Nitroaniline/2-Amino-3-Nitrofluorobenzene
  • 2-Fluoro-6-nitroaniline 98%
  • 2-Fluoro-6-nitroaniline98%
  • 2-Nitro-6-fluoroaniline
  • Einecs 241-779-9
  • 2-Amino-3-fluoronitrobenzene
CAS:
17809-36-8
MF:
C6H5FN2O2
MW:
156.11
EINECS:
241-779-9
Product Categories:
  • Miscellaneous
  • Benzenes
Mol File:
17809-36-8.mol
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2-FLUORO-6-NITRO-PHENYLAMINE Chemical Properties

Melting point:
74-75
Boiling point:
271.5±20.0 °C(Predicted)
Density 
1.448±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
solid
pka
-1.76±0.25(Predicted)
color 
Yellow/orange
InChI
InChI=1S/C6H5FN2O2/c7-4-2-1-3-5(6(4)8)9(10)11/h1-3H,8H2
InChIKey
BHWHYGWMNMCXBA-UHFFFAOYSA-N
SMILES
C1(N)=C([N+]([O-])=O)C=CC=C1F
CAS DataBase Reference
17809-36-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
29214990
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2-FLUORO-6-NITRO-PHENYLAMINE Usage And Synthesis

Chemical Properties

light yellow powder

Uses

2-Fluoro-6-nitro-phenylamine is mainly used as a pharmaceutical intermediate for the synthesis of specific drug molecules, such as anti-tumor drugs, antibacterial agents, etc.

Synthesis

342-52-9

17809-36-8

General procedure for the synthesis of 2-fluoro-6-nitroaniline from N-(2-fluoro-6-nitrophenyl)acetamide: 3 g (0.0151 mol) of N-(2-fluoro-6-nitrophenyl)acetamide (3a) was dissolved in 30 mL of concentrated H2SO4 and the reaction was stirred for 2 hr at 50 °C. After completion of the reaction, it was cooled to room temperature and the reaction solution was slowly poured into an ice bath and a large amount of precipitate was observed to be generated. The precipitate was collected by filtration and the acidic aqueous solution was extracted with ether. Purification by fast column chromatography afforded the target compound 2-fluoro-6-nitroaniline in 74% yield. The melting point of the product was 47-48 °C. 1H NMR (DMSO-d6) data: δ 7.82 (d, 1H, J=8.8 Hz, H-5), 7.42 (m, 1H, H-3), 7.25 (s, 2H, NH2), 6.63 (m, 1H, H-4). GC/MS analysis showed the molecular ion peak as 157 (M+H). Elemental analysis (C6H5FN2O2) Calculated values: C, 46.16; H, 3.23; F, 12.17; N, 17.94. Measured values: C, 46.18; H, 3.27; F, 12.15; N, 17.98.

References

[1] European Journal of Medicinal Chemistry, 2019, vol. 161, p. 399 - 415
[2] Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1976, vol. 30, p. 141 - 149

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