Identification | More | [Name]
Aminopyrazine | [CAS]
5049-61-6 | [Synonyms]
2-AMINOPYRAZINE AMINOPYRAZINE APZ NSC 13147 PYRAZIN-2-AMINE PYRAZIN-2-YLAMINE PYRAZINAMINE PYRAZINEAMINE TIMTEC-BB SBB004388 1,2-Dihydro-2-iminopyrazine 2-Pyrazinamine ENT 60202 Pyrazine, 1,2-dihydro-2-imino- Pyrazine, 2-amino- Pyrazine, amino- 2-Aminopyrazine,99% Aminopyrazine, 99+% 2-Piperazinamine 2-AMINOPYRAZINE 99% 2-Pyrazinylamine | [EINECS(EC#)]
225-748-7 | [Molecular Formula]
C4H5N3 | [MDL Number]
MFCD00006137 | [Molecular Weight]
95.1 | [MOL File]
5049-61-6.mol |
Chemical Properties | Back Directory | [Appearance]
SLIGHTLY YELLOW TO BEIGE CRYSTALLINE POWDER | [Melting point ]
118-120 °C (lit.) | [Boiling point ]
167.6°C (rough estimate) | [density ]
1.1031 (rough estimate) | [refractive index ]
1.5200 (estimate) | [storage temp. ]
Flammables area | [solubility ]
soluble in Methanol | [form ]
Crystalline Powder | [pka]
3.22±0.10(Predicted) | [color ]
Slightly yellow to beige | [Water Solubility ]
soluble | [Detection Methods]
HPLC,NMR | [BRN ]
107025 | [InChIKey]
XFTQRUTUGRCSGO-UHFFFAOYSA-N | [LogP]
-0.070 | [CAS DataBase Reference]
5049-61-6(CAS DataBase Reference) | [NIST Chemistry Reference]
Aminopyrazine(5049-61-6) |
Safety Data | Back Directory | [Hazard Codes ]
Xi,F | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . R11:Highly Flammable. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [HS Code ]
29339990 |
Hazard Information | Back Directory | [Chemical Properties]
SLIGHTLY YELLOW TO BEIGE CRYSTALLINE POWDER | [Application]
2-Aminopyrazine is a synthetic intermediate useful for pharmaceutical synthesis. It is used to synthesize favipiravir and substrate in a four-component synthesis of imidazolidines. | [Uses]
2-Aminopyrazine acts as a raw material in a four-component synthesis of imidazolidines. It is also used as an intermediate in synthetic chemistry. In addition, 2-aminopyrazine can be reacted with α-ketohydroximoyl chlorides to form 3-nitrosoimidazo[1,2-a]pyrazines. | [Definition]
ChEBI: Aminopyrazine is a member of pyrazines. |
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