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2-Amino-4-chloropyridine

CAS No.
19798-80-2
Chemical Name:
2-Amino-4-chloropyridine
Synonyms
4-CHLOROPYRIDIN-2-AMINE;4-chloro-2-pyridinamine;4-CHLORO-PYRIDINE-2-YLAMINE;DK765;cas:19798-80-2;IFLAB-BB F1926-0004;4-Chloropyrid-2-ylaMine;4-Chloro-2-amine-pyridin;2-Amino-4-Cholropyridine;4-Chloropyridine-2-amine
CBNumber:
CB7183078
Molecular Formula:
C5H5ClN2
Molecular Weight:
128.56
MDL Number:
MFCD04113820
MOL File:
19798-80-2.mol
MSDS File:
SDS
Last updated:2025-04-12 23:00:59

2-Amino-4-chloropyridine Properties

Melting point 126-127°C
Boiling point 240.8±20.0 °C(Predicted)
Density 1.326±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility DMSO, Methanol
form Liquid
pka 5.72±0.11(Predicted)
color Colorless to yellow to brown
λmax 294nm(CHCl3)(lit.)
Sensitive Air & Moisture Sensitive
InChI InChI=1S/C5H5ClN2/c6-4-1-2-8-5(7)3-4/h1-3H,(H2,7,8)
InChIKey RQMWVVBHJMUJNZ-UHFFFAOYSA-N
SMILES C1(N)=NC=CC(Cl)=C1
CAS DataBase Reference 19798-80-2(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

NFPA 704
1
2 0

2-Amino-4-chloropyridine price More Price(46)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 676020 2-Amino-4-chloropyridine 97% 19798-80-2 5g $70.1 2024-06-20 Buy
Sigma-Aldrich 676020 2-Amino-4-chloropyridine 97% 19798-80-2 25g $195 2024-06-20 Buy
TCI Chemical A2152 2-Amino-4-chloropyridine >98.0%(GC)(T) 19798-80-2 5g $79 2025-03-01 Buy
TCI Chemical A2152 2-Amino-4-chloropyridine >98.0%(GC)(T) 19798-80-2 25g $237 2025-03-01 Buy
Alfa Aesar H59130 2-Amino-4-chloropyridine, 97% 19798-80-2 5g $54.65 2025-03-01 Buy
Product number Packaging Price Buy
676020 5g $70.1 Buy
676020 25g $195 Buy
A2152 5g $79 Buy
A2152 25g $237 Buy
H59130 5g $54.65 Buy

2-Amino-4-chloropyridine Chemical Properties,Uses,Production

Chemical Properties

Light yellow Cryst

Uses

2-Amino-4-chloropyridine is a useful precursor that could be used to synthesize 2-amino-4,5-dichloropyridine, 2-amino-3,4-dichloropyridine, and 2-amino-3,4,5-trichloropyridine[1].

Synthesis Reference(s)

The Journal of Organic Chemistry, 72, p. 4554, 2007 DOI:

Synthesis

Methyl 4-chloropicolinate hydrochloride in methanol was treated with hydrazine hydrate, resulting in the formation of a precipitate. The suspension was then stirred for 2 hours and the precipitated hydrazide was collected through filtration. The hydrazide was dissolved in 1N hydrochloric acid and the solution was cooled to a temperature between 0-5 ℃. A solution of sodium nitrite in water was then added dropwise, causing another precipitate to form. After stirring for 15 minutes, the precipitate was collected by filtration and washed with water. The moist precipitate was then combined with a mixture of acetic acid and water, and the resulting solution was heated in a steam bath until gas evolution stopped. The reaction mixture was cooled to room temperature, the pH was adjusted to 7, and the resulting precipitate was collected via filtration. Recrystallization using ethanol yielded 2-Amino-4-chloropyridine in the form of a white crystalline solid[1].

References

[1] Gudmundsson, Kristjan S. , et al. "An Improved Large Scale Synthesis of 2-Amino-4-chloropyridine and Its Use for the Convenient Preparation of Various Polychlorinated 2-Aminopyridines." Synthetic Communications 27.5(1997):861-870.

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