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4-Iodopyridine

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CAS:15854-87-2
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4-Iodopyridine manufacturers

  • 4-Iodopyridine
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  • 2025-11-18
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  • Purity: 99.00%
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  • 4-iodopyridine
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  • 2023-04-21
  • CAS:15854-87-2
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  • Purity: 98%
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4-Iodopyridine Basic information
Product Name:4-Iodopyridine
Synonyms:BUTTPARK 96\50-18;4-IODOPYRIDINE;p-iodopyridine;SPECS AC-907/25004389;TIMTEC-BB SBB009104;4-Iodopyride;4-Iodopyridine 96%;4-lodopyridine
CAS:15854-87-2
MF:C5H4IN
MW:205
EINECS:640-182-4
Product Categories:Pharmaceutical intermediates;Halopyridines;Iodopyridines;Halogenated;Organohalides;Pyridines, Pyrimidines, Purines and Pteredines;pharmacetical;Halides;Pyridine;Pyridines derivates;blocks;Iodides;Pyridines
Mol File:15854-87-2.mol
4-Iodopyridine Structure
4-Iodopyridine Chemical Properties
Melting point 94-99 °C
Boiling point 212~215℃
density 1.081g/cm3
refractive index 1.5290
storage temp. -20°C
solubility soluble in Methanol
form Crystals or Powder
pkapK1:4.02(+1) (20°C)
color Pale brown to dark green-brown
Sensitive Light Sensitive
BRN 1594
InChIInChI=1S/C5H4IN/c6-5-1-3-7-4-2-5/h1-4H
InChIKeyRTLUPHDWSUGAOS-UHFFFAOYSA-N
SMILESC1=NC=CC(I)=C1
CAS DataBase Reference15854-87-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-41-37/38-22
Safety Statements 26-36-39
WGK Germany 3
Hazard Note Irritant/Light Sensitive
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
ALFA English
4-Iodopyridine Usage And Synthesis
Chemical PropertiesWhite to off-white crystals,turns brown on storage
Uses4-Iodopyridine is used as a reagent in the synthesis of indazolylamides as glucocorticoid receptor agonists.
Synthesis
Pyridine

110-86-1

4-Iodopyridine

15854-87-2

GENERAL METHODS: [Li(TMP)Zn(tBu)2] 1 was prepared according to literature methods in a 0.4 mmol scale solution of THF. Pyridine (0.032 mL, 0.4 mmol) was added to this solution at 0°C and the resulting light orange colored reaction mixture was allowed to stir for 2 h at room temperature. Subsequently, the reaction was quenched with I2 (508 mg, dissolved in 1 mL THF) and stirring was continued for 1 hour. A 10% Na2S2O3 solution was added until the color of the reaction mixture faded, and then the product was extracted with DCM (3 x 1 mL). The organic extracts were combined, dried with MgSO4 and concentrated under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography using EtOAc:heptane (20:80→30:70) as eluent to afford 4-iodopyridine (compound 5a) as an off-white solid (42 mg, 50% yield).1H NMR (400 MHz, CDCl3) δ ppm 7.59-7.86 (m, 2H), 8.07-8.44 (m 2H).

References[1] Tetrahedron Letters, 2011, vol. 52, # 36, p. 4590 - 4594
[2] Journal of Organic Chemistry, 1984, vol. 49, # 20, p. 3857 - 3859
Tag:4-Iodopyridine(15854-87-2) Related Product Information
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