Basic information Safety Supplier Related

3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID

Basic information Safety Supplier Related

3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID Basic information

Product Name:
3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID
Synonyms:
  • RARECHEM AK HC T305
  • 3-amino-3-(2-fluorophenyl)propanoic acid(SALTDATA: FREE)
  • 3-Amino-3-(2-fluorophenyl)propanoicacid95%
  • (RS)-3-Amino-3-(2-fluorophenyl)-propionic acid
  • DL-3-Amino-3-(2-fluorophenyl)propanoic acid
  • 3-AMINO-3-(2-FLUOROPHENYL)PROPANOIC ACID
  • 3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID
  • DL-3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID
CAS:
117391-49-8
MF:
C9H10FNO2
MW:
183.18
EINECS:
604-604-1
Product Categories:
  • B-Amino
Mol File:
117391-49-8.mol
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3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID Chemical Properties

Melting point:
222-224
Boiling point:
302.6±32.0 °C(Predicted)
Density 
1.289±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
3.67±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2922390090
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3-AMINO-3-(2-FLUORO-PHENYL)-PROPIONIC ACID Usage And Synthesis

Synthesis

141-82-2

446-52-6

117391-49-8

GENERAL METHOD: Malonic acid (1.04 g, 10 mmol) and ammonium formate (1.26 g, 20 mmol) were dissolved in ethanol (50 mL), followed by the addition of 2-fluorobenzaldehyde (10 mmol). The reaction mixture was heated to reflux for 7 hours. After completion of the reaction, it was cooled to room temperature and the crude product was collected by filtration. The crude product was purified by recrystallization (using 95% ethanol as a solvent) to give 3-amino-3-(2-fluorophenyl)propionic acid as a final white solid.

References

[1] European Journal of Medicinal Chemistry, 2018, vol. 143, p. 402 - 418
[2] Advanced Synthesis and Catalysis, 2010, vol. 352, # 2-3, p. 395 - 406
[3] Advanced Synthesis and Catalysis, 2017, vol. 359, # 9, p. 1570 - 1576
[4] ACS Medicinal Chemistry Letters, 2014, vol. 5, # 11, p. 1207 - 1212
[5] Journal of Organic Chemistry, 2009, vol. 74, # 23, p. 9152 - 9157

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