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5-Amino-2,3-dichloropyridine

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5-Amino-2,3-dichloropyridine Basic information

Product Name:
5-Amino-2,3-dichloropyridine
Synonyms:
  • 3-AMINO-5,6-DICHLOROPYRIDINE
  • 5,6-DICHLORO-PYRIDIN-3-YLAMINE
  • 5-AMINO-2,3-DICHLOROPYRIDINE
  • 2,3-DICHLORO-5-AMINOPYRIDINE
  • 2,3-DICHLORO-5-ANIMO-PYRIDINE
  • 5,6-Dichloropyridin-3-amine
  • 5-Amino-2,3-dichloropyridine ,97%
  • 5,6-Dichloro-3-pyridinamine
CAS:
98121-41-6
MF:
C5H4Cl2N2
MW:
163
Product Categories:
  • Heterocycle-Pyridine series
  • Boronic Acid
  • Building Blocks
  • C5
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Pyridines
  • Pyridine
  • Pyridines, Pyrimidines, Purines and Pteredines
Mol File:
98121-41-6.mol
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5-Amino-2,3-dichloropyridine Chemical Properties

Melting point:
107-112 °C
Boiling point:
321.3±37.0 °C(Predicted)
Density 
1.497±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
0.88±0.10(Predicted)
form 
powder to crystal
color 
White to Light yellow to Light orange
InChIKey
XTCHZNJJTQACES-UHFFFAOYSA-N
CAS DataBase Reference
98121-41-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
36/37/38-41-37/38-25
Safety Statements 
26-36/37-36-45-39
RIDADR 
2811
WGK Germany 
3
HazardClass 
6.1
PackingGroup 
HS Code 
29333999
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5-Amino-2,3-dichloropyridine Usage And Synthesis

Chemical Properties

Light yellow powder

Uses

5-Amino-2,3-dichloropyridine is a useful research reagent for organic synthesis.

Synthesis

22353-40-8

7439-89-6

98121-41-6

Example 10 Synthesis of 5-amino-2,3-dichloropyridine: 77.2 g (0.4 mol) of 2,3-dichloro-5-nitropyridine was dissolved in 135 mL of glacial acetic acid and 800 mL of water was slowly added under stirring conditions. Subsequently, 111.7 g (2 mol) of iron powder was added in batches, and the reaction temperature was controlled not to exceed 50 °C. After completion of the reaction, the mixture was filtered and the filtrate was extracted using ethyl acetate. The extracted organic phase was washed with water to neutral and subsequently dried with anhydrous magnesium sulfate and concentrated by rotary evaporator. The final product was purified by recrystallization from toluene to obtain 85% yield with a melting point of 107 °C.

References

[1] Patent: US4756739, 1988, A
[2] Patent: US5922732, 1999, A

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