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Iodopyrazine

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Iodopyrazine Basic information

Product Name:
Iodopyrazine
Synonyms:
  • IODOPYRAZINE
  • 2-IODOPYRAZINE 97%
  • Iodopyrazine,97%
  • 2-Iodo-1,4-diazine
  • 2-Iodopyrazine,95%
  • 2-IODOPYRAZINE
  • Iodopyrazine 97%
  • Iodopyrazine>
CAS:
32111-21-0
MF:
C4H3IN2
MW:
205.98
Product Categories:
  • alkyl Iodine
  • Building Blocks
  • Chemical Synthesis
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Organohalides
  • Pyrazine
  • PyrazinesHeterocyclic Building Blocks
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyrazines
  • Halogenated
Mol File:
32111-21-0.mol
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Iodopyrazine Chemical Properties

Melting point:
90 °C (decomp)
Boiling point:
109-110 °C34 mm Hg(lit.)
Density 
2.086 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.655(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-0.85±0.10(Predicted)
form 
Crystalline Powder
color 
White to pale yellow
Sensitive 
Light Sensitive
InChI
InChI=1S/C4H3IN2/c5-4-3-6-1-2-7-4/h1-3H
InChIKey
OYWPFIUVDKHHGQ-UHFFFAOYSA-N
SMILES
C1(I)=NC=CN=C1
CAS DataBase Reference
32111-21-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29339900

MSDS

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Iodopyrazine Usage And Synthesis

Chemical Properties

Colorless to brown liquid

Synthesis

14508-49-7

32111-21-0

General procedure for the synthesis of 2-iodopyrazine from 2-chloropyrazine: a reaction mixture of 2-chloropyrazine (7.5 mL, 83 mmol), NaI (30.3 g, 202 mmol), HOAc (9.6 mL, 168 mmol) and H2SO4 (0.5 mL) in MeCN (105 mL) was heated and refluxed for 4.5 hours. Upon completion of the reaction, the solvent was removed under reduced pressure and water (120 mL) was added. The solution was alkalized with saturated NaHCO3 solution and extracted with dichloromethane (DCM) (2 x 125 mL). The DCM layers were combined, washed sequentially with saturated Na2S2O3 solution and brine, and dried over anhydrous Na2SO4. The solvent was removed under reduced pressure to give the crude 2-iodopyrazine as an oil (12.33 g, 20% yield, 71% purity).1H NMR analysis showed that the crude contained less than about 10 mol% of 2-chloropyrazine. Following the same procedure, another batch of 2-chloropyrazine (50 g, 437 mmol) was converted to the crude 2-iodopyrazine (~65 g). The two crude batches were combined and distilled under reduced pressure (ca. 0.75 Torr, boiling point 47 °C) to give 64 g of pure 2-iodopyrazine (60% yield).1H-NMR (CDCl3, 300 MHz) δ 8.40 (dd, J = 1.8, 2.4 Hz, 1H), 8.51 (d, J = 2.4 Hz, 1H), 8.87 (d, J = 1.5 Hz, 1H).

References

[1] Tetrahedron, 1998, vol. 54, # 33, p. 9701 - 9710
[2] Patent: WO2009/114313, 2009, A2. Location in patent: Page/Page column 15

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