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4-AMINO-3-FLUOROBENZOIC ACID

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4-AMINO-3-FLUOROBENZOIC ACID Basic information

Product Name:
4-AMINO-3-FLUOROBENZOIC ACID
Synonyms:
  • 4-amino-3-fluoro-benzoicaci
  • 4-AMINO-3-FLUOROBENZENECARBOXYLIC ACID
  • 4-AMINO-3-FLUOROBENZOIC ACID
  • BUTTPARK 44\09-60
  • 3-FLUORO-4-AMINOBENZOIC ACID
  • 4-Amino-3-Fluorobenzoic
  • NSC 25758
  • 4-AMINO-3-FLUOROBENZ
CAS:
455-87-8
MF:
C7H6FNO2
MW:
155.13
EINECS:
207-250-1
Product Categories:
  • Fluorine series
  • Aromatics
  • Benzoic acid
  • Amines
  • blocks
  • Carboxes
  • FluoroCompounds
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Aromatics Compounds
Mol File:
455-87-8.mol
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4-AMINO-3-FLUOROBENZOIC ACID Chemical Properties

Melting point:
215-218°C
Boiling point:
320.8±27.0 °C(Predicted)
Density 
1.430±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Hot Water
form 
Fine Needles
pka
4.52±0.10(Predicted)
color 
White to Light yellow to Light orange
InChIKey
JSKXHTHMCCDEGD-UHFFFAOYSA-N
CAS DataBase Reference
455-87-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
RTECS 
DG2525000
HazardClass 
IRRITANT
HS Code 
2922498590
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4-AMINO-3-FLUOROBENZOIC ACID Usage And Synthesis

Chemical Properties

Fine Needles

Synthesis

403-21-4

455-87-8

In a 1000 mL round-bottomed single-necked flask, 3-fluoro-4-nitrobenzoic acid (30 g, 190 mmol) was dissolved in 300 mL of a solvent mixture of methanol and tetrahydrofuran, and carbon-loaded palladium (2 g) was added as a catalyst. The reaction system was charged with hydrogen and the reaction was stirred at room temperature for 15 hours. Upon completion of the reaction, the reaction mixture was filtered through diatomaceous earth and the filtrate was collected. The filtrate was dried to give a white solid product. The white solid was further dried in an oven to finally obtain 3-fluoro-4-aminobenzoic acid (24.86 g, 98.6% yield).

References

[1] Patent: CN105294567, 2016, A. Location in patent: Paragraph 0033-0036
[2] Tetrahedron, 2018, vol. 74, # 47, p. 6795 - 6803
[3] Journal of the American Chemical Society, 1944, vol. 66, p. 1631
[4] Bioorganic and Medicinal Chemistry, 2016, vol. 24, # 12, p. 2697 - 2706

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