ChemicalBook--->CAS DataBase List--->21943-15-7

21943-15-7

21943-15-7 Structure

21943-15-7 Structure
IdentificationBack Directory
[Name]

3,5-Dibromo-2-hydroxypyrazine
[CAS]

21943-15-7
[Synonyms]

3,5-bromopyrazin-2-ol
3,5-DIBROMO-PYRAZIN-2-OL
3,5-dibromo-1H-pyrazin-2-one
3,5-dibromo-2(1H)-Pyrazinone
2-Hydroxy-3,5-dibromopyrazine
3,5-DIBROMO-2-HYDROXYPYRAZINE
2(1H)-Pyrazinone, 3,5-dibromo-
3,5-DibroMo-2-hydroxypyrazine, 95+%
3,5-Dibromo-2-hydroxypyrazine ISO 9001:2015 REACH
[Molecular Formula]

C4H2Br2N2O
[MDL Number]

MFCD07371406
[MOL File]

21943-15-7.mol
[Molecular Weight]

253.88
Chemical PropertiesBack Directory
[Melting point ]

174-178°C
[density ]

2.53±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[pka]

8.35±0.60(Predicted)
[Appearance]

Light yellow to yellow Solid
[InChI]

InChI=1S/C4H2Br2N2O/c5-2-1-7-4(9)3(6)8-2/h1H,(H,7,9)
[InChIKey]

NHVGHXUOFWEOSN-UHFFFAOYSA-N
[SMILES]

C1(=O)NC=C(Br)N=C1Br
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H318
[Precautionary statements ]

P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22-41
[Safety Statements ]

26-39
[WGK Germany ]

1
[HS Code ]

29339900
[Storage Class]

13 - Non Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Uses]

3,5-Dibromo-pyrazinol ,is a pyrazine derivative that can be used as a potential building block in chemical synthesis. It can also be used in SRN1 mechanism in heteroaromatic nucleophilic substitution.
[Synthesis]

2-Amino-3,5-dibromopyrazine

24241-18-7

3,5-Dibromo-2-hydroxypyrazine

21943-15-7

Preparation of compound 36a: 3,5-dibromopyrazin-2-ol To a stirred solution of 3,5-dibromopyrazin-2-amine (30 g, 0.12 mol) in acetic acid (300 mL) was added sulfuric acid (50 mL) dropwise at 15-25 °C. Subsequently, a solution of sodium nitrite (16.6 g, 0.24 mol) in water (100 mL) was added dropwise to the resulting solution over a period of 1.5 hours at 10-15°C. After the dropwise addition was completed, the reaction mixture was continued to be stirred at 10-15 °C for 1 hour. The reaction mixture was poured into water (3L) and extracted with ethyl acetate (1L x 3). The organic layers were combined, washed sequentially with saturated sodium bicarbonate solution (1L×3) and brine (1L), dried with anhydrous sodium sulfate, and concentrated under reduced pressure to afford 3,5-dibromo-2-hydroxypyrazine (36a) as a yellow solid (24 g, 79.4% yield). 1H NMR (400 MHz, CDCl3): δ 7.44 (s, 1H).

[References]

[1] Patent: WO2010/16005, 2010, A1. Location in patent: Page/Page column 144
Spectrum DetailBack Directory
[Spectrum Detail]

3,5-Dibromo-2-hydroxypyrazine(21943-15-7)1HNMR
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