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2-Amino-5-fluorobenzonitrile

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2-Amino-5-fluorobenzonitrile Basic information

Product Name:
2-Amino-5-fluorobenzonitrile
Synonyms:
  • 5-FLUOROANTHRANILONITRILE
  • 5-FLUOROANTHRONILONITRILE
  • 2-AMINO-5-FLUOROBENZONITRILE
  • 2-AMINO-5-FLUOROBENONITRILE
  • 2-Amino-5-fluorobenzonitrile 98+%
  • 2-Cyano-4-fluoroaniline, 5-Fluoroanthranilonitrile
  • 2-AMino-5-fluorobenzonitrle
  • 2-AMino-5-fluorobenzonitrile, 97+%
CAS:
61272-77-3
MF:
C7H5FN2
MW:
136.13
Product Categories:
  • Fluorine series
  • Aryl Fluorinated Building Blocks
  • Building Blocks
  • C6 to C7
  • C7
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Nitrogen Compounds
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Other Fluorinated Organic Building Blocks
  • C6 to C7
  • Cyanides/Nitriles
  • Nitrogen Compounds
  • Aromatic Nitriles
Mol File:
61272-77-3.mol
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2-Amino-5-fluorobenzonitrile Chemical Properties

Melting point:
92-96 °C (lit.)
Boiling point:
138 °C/15 mmHg (lit.)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
powder
pka
1.87±0.10(Predicted)
color 
Faint yellow to faint brown
CAS DataBase Reference
61272-77-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20/21/22
Safety Statements 
22-24/25
RIDADR 
3439
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
2926907090

MSDS

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2-Amino-5-fluorobenzonitrile Usage And Synthesis

Uses

2-Amino-5-fluorobenzonitrile is a key intermediate.

Chemical Properties

white to light yellow crystal powder

Synthesis

756839-23-3

61272-77-3

GENERAL METHODS: Azide-based compounds (1 mmol) were added to an aqueous solution (5 mL) containing freshly prepared Fe(0) nanoparticles (3 mmol) at room temperature and under argon atmosphere. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was extracted with ethyl acetate (3 × 10 mL), ensuring that all Fe-containing material was retained around the stir bar. Subsequently, the solvent in the organic phase was evaporated and the crude product was purified by short column chromatography. The final product was structurally confirmed by infrared spectroscopy (IR), proton nuclear magnetic resonance (1H NMR) and carbon nuclear magnetic resonance (13C NMR) data.

References

[1] Tetrahedron Letters, 2017, vol. 58, # 35, p. 3457 - 3460

2-Amino-5-fluorobenzonitrile Preparation Products And Raw materials

Preparation Products

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