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Iodopyrazine

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CAS:32111-21-0
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CAS:32111-21-0
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Iodopyrazine manufacturers

  • Iodopyrazine
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  • $1.10 / 1g
  • 2025-11-18
  • CAS:32111-21-0
  • Min. Order: 1g
  • Purity: 99.00%
  • Supply Ability: 100 Tons
  • Iodopyrazine
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  • 2020-04-30
  • CAS:32111-21-0
  • Min. Order: 1KG
  • Purity: 99.0%+
  • Supply Ability: 800 tons
  • Iodopyrazine
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  • $1.00 / 1KG
  • 2019-07-06
  • CAS:32111-21-0
  • Min. Order: 1KG
  • Purity: 99%
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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
EINECS:
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
Iodopyrazine Structure
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.)
Fp >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
InChIInChI=1S/C4H3IN2/c5-4-3-6-1-2-7-4/h1-3H
InChIKeyOYWPFIUVDKHHGQ-UHFFFAOYSA-N
SMILESC1(I)=NC=CN=C1
CAS DataBase Reference32111-21-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
Hazard Note Irritant
HS Code 29339900
MSDS Information
ProviderLanguage
SigmaAldrich English
Iodopyrazine Usage And Synthesis
Chemical PropertiesColorless to brown liquid
Synthesis
2-Chloropyrazine

14508-49-7

Iodopyrazine

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
Tag:Iodopyrazine(32111-21-0) Related Product Information
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