PYRAZINE N-OXIDE

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Company Name: Dayang Chem (Hangzhou) Co.,Ltd.
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Products Intro: Product Name:Pyrazine N-oxide
CAS:2423-65-6
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Products Intro: Product Name:Pyrazine N-oxide
CAS:2423-65-6
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Company Name: GIHI CHEMICALS CO.,LIMITED
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Products Intro: Product Name:Pyrazine N-oxide
CAS:2423-65-6
Purity:99 Package:5KG;1KG,25kg
Company Name: Aladdin Scientific
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Products Intro: Product Name:Pyrazine N-oxide
CAS:2423-65-6
Purity:97% Package:$19.9/250mg;$61.9/1g;$236.9/5g;Bulk package Remarks:97%
Company Name: Adamas Reagent, Ltd.  
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Products Intro: Product Name:Pyrazine 1-Oxide
CAS:2423-65-6
Purity:97%+ Package:1G;5G;10G;25G;50G;100G,1KG;25KG;50KG
PYRAZINE N-OXIDE Basic information
Product Name:PYRAZINE N-OXIDE
Synonyms:RARECHEM BG FB 0041;PYRAZINE N-OXIDE;Pyrazine N-oxide 97%;1-oxidopyrazin-1-ium;Pyrazine-1-oxide;Pyrazine N-oxide
CAS:2423-65-6
MF:C4H4N2O
MW:96.09
EINECS:
Product Categories:
Mol File:2423-65-6.mol
PYRAZINE N-OXIDE Structure
PYRAZINE N-OXIDE Chemical Properties
Melting point 112-116 °C
Boiling point 126-127 °C(Press: 14 Torr)
density 1.19±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form solid
pka0.45±0.39(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
Hazard Codes F,Xn
Risk Statements 11-22-37/38-41
Safety Statements 26-39
RIDADR UN 1325 4.1/PG 2
WGK Germany 3
MSDS Information
PYRAZINE N-OXIDE Usage And Synthesis
Synthesis
Pyrazine

290-37-9

PYRAZINE N-OXIDE

2423-65-6

General procedure 1: Diazine oxidation; Pyrazine (1 eq.) and mCPBA (1 eq.) were dissolved in DCM (0.2 M). The reaction mixture was stirred at room temperature for 16 hours. PPh3 (0.5 eq.) was then added to quench the unreacted peracid and stirring was continued for 4 hours. After completion of the reaction, the solvent was removed by concentration under reduced pressure and the residue was purified by silica gel column chromatography. The synthesis of pyrazine-N-oxide was carried out according to the general procedure 1 using 100% EtOAc as the initial eluent, followed by switching to 20% MeOH/EtOAc mixed solvent in a gradient elution to give a white solid product in 88% yield. The product was characterized as follows: 1H NMR (300 MHz, CDCl3, 293 K, TMS): δ 8.50 (2H, d, J = 3.9 Hz), 8.14 (2H, d, J = 4.8 Hz); 13C NMR (75 MHz, CDCl3, 293 K, TMS): 147.8, 134.0; HRMS (ESI) m/z calculated for C4H4N2O [M]+: 96.0324, found: 96.0295; mp: 103.2-104.5 °C; IR (νmax/cm-1): 3120, 3088, 1595, 861, 847, 838; Rf (20% MeOH/EtOAc): 0.3.

Purification MethodsIf the sample contains pyrazine-1-oxide, then place it in a Soxhlet extractor and extract it with hot pet ether (b 60-68o) in which the mono-oxide is soluble. Collect the dioxide from the thimble and recrystallise it from MeOH. It is dried in vacuo. It has at 1270cm-1 . [Koelsch & Gumprecht J Org Chem 23 1605 1958.]
References[1] Organic Letters, 2017, vol. 19, # 18, p. 4707 - 4709
[2] Organic Letters, 2018, vol. 20, # 8, p. 2346 - 2350
[3] Angewandte Chemie - International Edition, 2006, vol. 45, # 46, p. 7781 - 7786
[4] Patent: US2008/132698, 2008, A1. Location in patent: Page/Page column 17-18
[5] Chemical Communications, 2015, vol. 51, # 12, p. 2425 - 2428
PYRAZINE N-OXIDE Preparation Products And Raw materials
Raw materialsPyrazine-->Dichloromethane-->3-Chloroperoxybenzoic acid
Preparation ProductsPyrazinecarbonitrile, 6-amino- (9CI)
Tag:PYRAZINE N-OXIDE(2423-65-6) Related Product Information
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