| Identification | More | [Name]
5-Amino-2,3-dichloropyridine | [CAS]
98121-41-6 | [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% | [Molecular Formula]
C5H4Cl2N2 | [MDL Number]
MFCD03840434 | [Molecular Weight]
163 | [MOL File]
98121-41-6.mol |
| Chemical Properties | Back Directory | [Appearance]
Light yellow powder | [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 | [form ]
powder to crystal | [pka]
0.88±0.10(Predicted) | [color ]
White to Light yellow to Light orange | [Detection Methods]
HPLC,NMR | [InChIKey]
XTCHZNJJTQACES-UHFFFAOYSA-N | [CAS DataBase Reference]
98121-41-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S36:Wear suitable protective clothing . | [RIDADR ]
2811 | [WGK Germany ]
3 | [HazardClass ]
6.1 | [PackingGroup ]
Ⅲ | [HS Code ]
29333990 |
| Hazard Information | Back Directory | [Chemical Properties]
Light yellow powder | [Uses]
5-Amino-2,3-dichloropyridine is a useful research reagent for organic synthesis. | [Synthesis]
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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