Basic information Uses Uses Safety Supplier Related

2,2-Difluoropropionic acid

Basic information Uses Uses Safety Supplier Related

2,2-Difluoropropionic acid Basic information

Product Name:
2,2-Difluoropropionic acid
Synonyms:
  • 2,2-DIFLUOROPROPIONIC ACID
  • 2,2-Difluoropropanoic acid
  • 2,2-Difluoropropionic acid 97%
  • Propanoic acid, 2,2-difluoro-
CAS:
373-96-6
MF:
C3H4F2O2
MW:
110.06
Product Categories:
  • Carboxylic Acids
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Other Fluorinated Organic Building Blocks
  • Alkyl Fluorinated Building Blocks
  • Building Blocks
  • C1 to C5
  • Carbonyl Compounds
  • C1 to C5
  • Carbonyl Compounds
  • Carboxylic Acids
Mol File:
373-96-6.mol
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2,2-Difluoropropionic acid Chemical Properties

Melting point:
38-45 °C
Boiling point:
25-30 °C/5 mmHg
Density 
1.316±0.06 g/cm3(Predicted)
Flash point:
25-30°C/5mm
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to crystal
pka
1.34±0.10(Predicted)
color 
White to Almost white
InChI
InChI=1S/C3H4F2O2/c1-3(4,5)2(6)7/h1H3,(H,6,7)
InChIKey
PMWGIVRHUIAIII-UHFFFAOYSA-N
SMILES
C(O)(=O)C(F)(F)C
CAS DataBase Reference
373-96-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,C
Risk Statements 
34-36
Safety Statements 
26-36/37/39
RIDADR 
3261
WGK Germany 
3
HazardClass 
8
PackingGroup 
III
HS Code 
29159000
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2,2-Difluoropropionic acid Usage And Synthesis

Uses

2,2-Difluoropropionic acid is a useful research chemical.

Uses

2,2-Difluoropropionic acid is mainly used in biochemical research.

Chemical Properties

White powder

Synthesis

28781-85-3

373-96-6

The general procedure for synthesizing 2,2-difluoropropionic acid from ethyl 2,2-difluoropropionate was as follows: referring to Example G38, ethyl 2,2-difluoropropionate (1.2 g, 8.8 mmol) was dissolved in ethanol (26 mL), followed by the slow addition of 2N aqueous sodium hydroxide solution (26 mL). The reaction mixture was stirred at 0 °C, then gradually warmed to room temperature and continued stirring for 14 hours. Upon completion of the reaction, the reaction mixture was acidified to pH < 7 with 2N hydrochloric acid and then extracted with ether. The organic phases were combined, dried over anhydrous sodium sulfate and subsequently concentrated under reduced pressure to give 2,2-difluoropropionic acid (0.90 g, 92% yield). The product was an oil with the following 1H-NMR (CDCl3) data: δ 1.85 (3H, t, J = 19.0 Hz), 6.21 (1H, br s).

References

[1] Patent: EP1402900, 2004, A1
[2] Patent: US2004/53973, 2004, A1
[3] Journal of Organic Chemistry USSR (English Translation), 1981, vol. 17, p. 1260 - 1263
[4] Zhurnal Organicheskoi Khimii, 1981, vol. 17, # 7, p. 1417 - 1420
[5] Journal of Organic Chemistry USSR (English Translation), 1982, vol. 18, p. 1597 - 1601

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