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2-Amino-4,5-dichloropyridine

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Products Intro: Product Name:2-amino-4,5-dichloropyridine
CAS:188577-68-6
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:2-Amino-4,5-dichloropyridine
CAS:188577-68-6
Purity:0.99 Package:5KG;1KG
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Products Intro: Product Name:4,5-Dichloropyridin-2-amine
CAS:188577-68-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-05969
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Products Intro: Product Name:2-amino-4,5-dichloropyridine
CAS:188577-68-6
Purity:99% Package:1kg
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Products Intro: Product Name:2-Amino-4,5-dichloropyridine
CAS:188577-68-6
Purity:99% Package:1KG;1USD

2-Amino-4,5-dichloropyridine manufacturers

2-Amino-4,5-dichloropyridine Basic information
Product Name:2-Amino-4,5-dichloropyridine
Synonyms:2-AMINO-4,5-DICHLOROPYRIDINE;4,5-dichloropyridin-2-amine;2-Pyridinamine,4,5-dichloro-(9CI);2-AMINO-4,5-DICHLOROPYRIDINE 97%;REF DUPL: 2-amino-4,5-dichloropyridine;2-Pyridinamine, 4,5-dichloro-;4,5-Dichloro-pyridin-2-ylamine;4,5-Dichloro-2-pyridinamine
CAS:188577-68-6
MF:C5H4Cl2N2
MW:163
EINECS:
Product Categories:Pyridines;HALIDE
Mol File:188577-68-6.mol
2-Amino-4,5-dichloropyridine Structure
2-Amino-4,5-dichloropyridine Chemical Properties
Boiling point 269.8±35.0 °C(Predicted)
density 1.497±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka3.63±0.24(Predicted)
form powder
color Red brown
InChIInChI=1S/C5H4Cl2N2/c6-3-1-5(8)9-2-4(3)7/h1-2H,(H2,8,9)
InChIKeyCRRAQLWJVYODCL-UHFFFAOYSA-N
SMILESC1(N)=NC=C(Cl)C(Cl)=C1
Safety Information
Hazard Codes T
RIDADR UN2811
HS Code 2933399990
MSDS Information
2-Amino-4,5-dichloropyridine Usage And Synthesis
Synthesis
2-Amino-4-chloropyridine

19798-80-2

2-Amino-4,5-dichloropyridine

188577-68-6

General procedure for the synthesis of 4,5-dichloropyridin-2-amine from 2-amino-4-chloropyridine: N-chlorosuccinimide (NCS, 2.67 g, 20.0 mmol) was added to a solution of 2-amino-4-chloropyridine (1.28 g, 10.0 mmol) in DMF (40 mL) at -20 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 24 hours. Upon completion of the reaction, the mixture was poured into ice water (300 mL) and extracted with ethyl acetate. The combined organic phases were washed sequentially with 1 M sodium hydroxide solution and saturated saline, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford the target compound 4,5-dichloropyridin-2-amine (1.12 g, 69.0% yield).

References[1] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 1, p. 60 - 67
[2] European Journal of Medicinal Chemistry, 2016, vol. 117, p. 19 - 32
[3] Patent: WO2016/124553, 2016, A1. Location in patent: Page/Page column 71-72
[4] Patent: WO2018/11138, 2018, A1. Location in patent: Page/Page column 69-70
[5] Synthetic Communications, 1997, vol. 27, # 5, p. 861 - 870
Tag:2-Amino-4,5-dichloropyridine(188577-68-6) Related Product Information
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