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3-AMINOPYRAZINE-2-CARBONITRILE

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:3-Aminopyrazine-2-carbonitrile
CAS:25911-65-3
Purity:98% Min. Package:100g;1kg;5kg,10kg,25kg,50kg
Company Name: ATK CHEMICAL COMPANY LIMITED
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Products Intro: Product Name:3-aminopyrazine-2-carbonitrile
CAS:25911-65-3
Purity:98% Package:25G;50G;100G;500G;1KG;10KG;50KG
Company Name: Shenzhen Nexconn Pharmatechs Ltd
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Products Intro: Product Name:3-AMINOPYRAZINE-2-CARBONITRILE
CAS:25911-65-3
Purity:0.98 Package:1KG;10KG;50KG
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Products Intro: Product Name:3-AMINOPYRAZINE-2-CARBONITRILE
CAS:25911-65-3
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:3-Aminopyrazine-2-carbonitrile
CAS:25911-65-3
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-04896

3-AMINOPYRAZINE-2-CARBONITRILE manufacturers

3-AMINOPYRAZINE-2-CARBONITRILE Basic information
Product Name:3-AMINOPYRAZINE-2-CARBONITRILE
Synonyms:BUTTPARK 29\04-92;3-AMINOPYRAZINE-2-CARBONITRILE;2-aMino-3-cyanopyrazine;Pyrazinecarbonitrile, 3-amino-;3-Amino-2-pyrazinecarbonitrile;2-Pyrazinecarbonitrile, 3-amino-;3-AMINOPYRAZINE-2-CARBONITRILE ISO 9001:2015 REACH
CAS:25911-65-3
MF:C5H4N4
MW:120.11
EINECS:
Product Categories:Pyrazine
Mol File:25911-65-3.mol
3-AMINOPYRAZINE-2-CARBONITRILE Structure
3-AMINOPYRAZINE-2-CARBONITRILE Chemical Properties
Melting point 191.9 °C
Boiling point 364.8±42.0 °C(Predicted)
density 1.34±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka1.45±0.10(Predicted)
AppearanceLight brown to yellow Solid
Safety Information
MSDS Information
3-AMINOPYRAZINE-2-CARBONITRILE Usage And Synthesis
Uses3-Aminopyrazine-2-carbonitrile is a useful synthesis reagent.
Synthesis Reference(s)Journal of Heterocyclic Chemistry, 26, p. 817, 1989 DOI: 10.1002/jhet.5570260357
Synthesis
Pyrazinecarboxamide, 3-amino- (7CI,9CI)

32587-10-3

3-AMINOPYRAZINE-2-CARBONITRILE

25911-65-3

Example 3 Synthesis of 3-aminopyrazine-2-carbonitrile (Intermediate 2): Intermediate 1 (3-aminopyrazine-2-carboxamide, 3.5 g, 25 mmol) was dissolved in DMF (40 mL) at room temperature, followed by slow dropwise addition of POCl3 (4.5 mL, 49 mmol). The reaction mixture was heated at 80 °C with stirring for 15 min, after which it was cooled to room temperature. The reaction mixture was slowly poured into ice water and the pH was adjusted to neutral with 10% NaOH solution. The precipitated solid was collected by filtration and redissolved in 5% HCl solution. The acidic solution was heated at 70 °C for 30 min, followed by filtration to separate the solid product. The target compound 3-aminopyrazine-2-carbonitrile was obtained as a brown solid (1.7 g, 56% yield) after sufficient washing with water. The product was characterized by 1H NMR (500 MHz, DMSO-d6): δ 8.28 (d, J=2.4 Hz, 1H), 7.90 (d, J=2.4 Hz, 1H), 7.32 (br s, 2H). Mass spectrum (ES+): m/z 121 ([M+H]+).

References[1] Patent: US2007/259876, 2007, A1. Location in patent: Page/Page column 18
[2] Journal of the American Chemical Society, 1945, vol. 67, p. 1711
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 12, p. 3238 - 3242
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