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622392-04-5

622392-04-5 Structure

622392-04-5 Structure
IdentificationBack Directory
[Name]

2-BROMO-5-IODOPYRAZINE
[CAS]

622392-04-5
[Synonyms]

2-BROMO-5-IODOPYRAZINE
2-Iodo-5-bromo pyrazine
Pyrazine,2-broMo-5-iodo-
2-Bromo-5-iodopyrazine98%
2-Bromo-5-iodopyrazine 98%
2-Bromo-5-iodo-1,4-diazine
2-BROMO-5-IODOPYRAZINE ISO 9001:2015 REACH
[EINECS(EC#)]

201-903-5
[Molecular Formula]

C4H2BrIN2
[MDL Number]

MFCD08061602
[MOL File]

622392-04-5.mol
[Molecular Weight]

284.88
Chemical PropertiesBack Directory
[Melting point ]

95-97°C
[Boiling point ]

273.7±35.0 °C(Predicted)
[density ]

2.495±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

powder
[pka]

-4.29±0.10(Predicted)
[color ]

Beige
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

2-BROMO-5-IODOPYRAZINE(622392-04-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-5-bromopyrazine

59489-71-3

2-BROMO-5-IODOPYRAZINE

622392-04-5

General procedure for the synthesis of 2-bromo-5-iodopyrazine from 2-amino-5-bromopyrazine: to a solution of DME (30 mL) containing 2-amino-5-bromopyrazine (1.25 g, 7.2 mmol) was added sequentially CsI (1.86 g, 7.2 mmol), iodine (0.92 g, 3.6 mmol), CuI (0.42 g, 2.2 mmol) and isoamyl nitrite (5.8 mL, 43.2 mmol). The reaction mixture was heated to 60 °C and gas was observed to escape. After 35 min of reaction, the mixture was cooled to room temperature, extracted with saturated aqueous NH4Cl solution (100 mL) and EtOAc (100 mL) and filtered through diatomaceous earth. The organic layer was separated, washed with 5% Na2S2O3 solution, dried over MgSO4 and concentrated to give the yellow solid product 2-bromo-5-iodopyrazine (1.50 g, 74% yield).GC-MS analysis showed molecular ion peaks m/z of 284 and 286 (M+).

[References]

[1] Patent: WO2004/811, 2003, A1. Location in patent: Page 197-198
[2] Chemistry - A European Journal, 2003, vol. 9, # 22, p. 5597 - 5604
[3] Patent: WO2008/24390, 2008, A2. Location in patent: Page/Page column 58
[4] Patent: US2008/45539, 2008, A1. Location in patent: Page/Page column 25
[5] Patent: WO2010/122151, 2010, A1. Location in patent: Page/Page column 61
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