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2-AMINO-5-TRIFLUOROMETHYL-BENZOIC ACID

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2-AMINO-5-TRIFLUOROMETHYL-BENZOIC ACID Basic information

Product Name:
2-AMINO-5-TRIFLUOROMETHYL-BENZOIC ACID
Synonyms:
  • 2-AMINO-5-TRIFLUOROMETHYL-BENZOIC ACID
  • BUTTPARK 24\07-92
  • Benzoic acid, 2-amino-5-(trifluoromethyl)-
  • 4-Amino-3-carboxybenzotrifluoride, 2-Carboxy-4-(trifluoromethyl)aniline
  • 2-Amino-5-trifuloromethylbenzoic acid
  • 4-Amino-3-carboxybenzotrifluoride
  • 2-Amino-5-(trifluoromethyl)benzoic acid 98%
  • 2-Amino-5-(trifluoromethyl)benzoicacid,95%
CAS:
83265-53-6
MF:
C8H6F3NO2
MW:
205.1339496
EINECS:
207-163-9
Product Categories:
  • Fluorine series
  • Benzoic acid series
Mol File:
83265-53-6.mol
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2-AMINO-5-TRIFLUOROMETHYL-BENZOIC ACID Chemical Properties

Melting point:
141-146℃
Boiling point:
301.6±42.0 °C(Predicted)
Density 
1.489±0.06 g/cm3(Predicted)
Flash point:
>110°(230°F)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
Solid
pka
4.51±0.10(Predicted)
Appearance
White to light yellow Solid
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2916399090
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2-AMINO-5-TRIFLUOROMETHYL-BENZOIC ACID Usage And Synthesis

Uses

2-amino-5-(trifluoromethyl)benzoic Acid is a benzoic acid derivative whose molecular structure contains substituents amino and trifluoromethyl at positions 2 and 5. The substance can be used to prepare small molecule inhibitors or anticancer drugs, and is widely used in fields such as chemical or pharmaceutical manufacturing.

Synthesis

1214373-54-2

83265-53-6

Step 2 Synthesis of 2-amino-5-(trifluoromethyl)benzoic acid: 2-nitro-5-(trifluoromethyl)benzoic acid (1.2 g, 4.78 mmol) was suspended in ethanol (10 mL) and 10% Pd/C catalyst (120 mg) was added. The hydrogenation reaction was carried out at room temperature and atmospheric pressure for 1 hour. Upon completion of the reaction, the catalyst was removed by filtration through a diatomaceous earth pad and the filtrate was concentrated to afford 2-amino-5-(trifluoromethyl)benzoic acid (900 mg, 85.2% yield) as a pale white solid. The resulting product could be used in subsequent reactions without further purification.

References

[1] Patent: WO2016/23826, 2016, A1. Location in patent: Page/Page column 52; 53

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