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2-AMINO-5-PHENYLPYRIDINE

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2-AMINO-5-PHENYLPYRIDINE Basic information

Product Name:
2-AMINO-5-PHENYLPYRIDINE
Synonyms:
  • 2-amino-5-phenyl-pyridin
  • 5-PHENYL-2-PYRIDINAMINE
  • 5-PHENYL-PYRIDIN-2-YLAMINE
  • AKOS BAR-1613
  • 2-AMINO-5-PHENYLPYRIDINE
  • PHE-P-1
  • 2-Amino-5-phenylpyridine,97%
  • 2-pyridinaMine, 5-phenyl-
CAS:
33421-40-8
MF:
C11H10N2
MW:
170.21
Product Categories:
  • Amines
  • Heterocycles
  • pharmacetical
  • Aromatics Compounds
  • Aromatics
Mol File:
33421-40-8.mol
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2-AMINO-5-PHENYLPYRIDINE Chemical Properties

Melting point:
132 °C
Boiling point:
324℃
Density 
1.133
refractive index 
1.5200 (estimate)
Flash point:
176℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
pka
6.32±0.13(Predicted)
color 
Off-White to Light Yellow
CAS DataBase Reference
33421-40-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-36-22-40
Safety Statements 
26-36/37/39-36/37
RTECS 
US2145000
HS Code 
29333990
Toxicity
mma-sat 100 mg/plate CPBTAL 26,611,78
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2-AMINO-5-PHENYLPYRIDINE Usage And Synthesis

Chemical Properties

Beige Crystalline Solid

Uses

A product from the pyrolysis of phenylalanine

Definition

ChEBI: 5-Phenyl-2-pyridinamine is a phenylpyridine.

Safety Profile

Mutation data reported. Whenheated to decomposition it emits toxic fumes of NOx.

Synthesis

66600-05-3

33421-40-8

The general procedure for the synthesis of 2-amino-5-phenylpyridine from 2-chloro-5-phenylpyridine is as follows: 1. a solution was prepared by dissolving 2-chloro-5-phenylpyridine (4.0 g, 0.021 mol) in anhydrous ether (160 ml). 2. the above solution was slowly added dropwise to a solution of liquid ammonia (160 ml) containing sodium (3.39 g, 0.15 g atoms) and ferrous nitrate hexahydrate (0.095 g). 3. The resulting suspension was heated to reflux for 4 hours. 4. Upon completion of the reaction, ammonium chloride was added and the ammonia was allowed to evaporate naturally. 5. The residue is treated with a 5% aqueous sodium hydroxide solution (5 mL). 6. Filter the mixture to separate the solids from the liquid. 7. Extract the aqueous layer with ether (2 x 100 ml) and combine the ether layers. 8. Wash the combined ether layers with brine and dry with sodium sulfate. 9. The dried ether solution was concentrated to give the crude product. 10. the crude product was recrystallized with methylcyclohexane. 11. 11. The recrystallized product was ground with chloroform (100 ml). 12. The mixture was filtered and the filtrate was evaporated to give the final product 2-amino-5-phenylpyridine (1.3 g, 36% yield) with a melting point of 205 °C. Melting points of 133°-135° have been reported in the literature (Chem. Ber., 91, 247 (1958)).

References

[1] Patent: US4122274, 1978, A

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