2-Bromo-5-iodopyridine Chemical Properties

Melting point:

121-123 °C (lit.)

Boiling point:

278.6±20.0 °C(Predicted)

Density 

2.347±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

pka

-1.23±0.10(Predicted)

form 

Powder

color 

White to off-white

Sensitive 

Light Sensitive

BRN 

109100

InChI

InChI=1S/C5H3BrIN/c6-5-2-1-4(7)3-8-5/h1-3H

InChIKey

LLKRSJVPTKFSLS-UHFFFAOYSA-N

SMILES

C1(Br)=NC=C(I)C=C1

CAS DataBase Reference

73290-22-9(CAS DataBase Reference)

Safety Information

Hazard Codes 

Xn,Xi

Risk Statements 

22-37/38-41

Safety Statements 

26-36/39

WGK Germany 

3

HazardClass 

IRRITANT

HS Code 

29333990

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ALFA

2-Bromo-5-iodopyridine Usage And Synthesis

Chemical Properties

White crystalline

Uses

2-Bromo-5-iodopyridine can be used to develop fluorescent compounds (manisyl-substituted terpyridine, bipyridine, and phenanthroline). It is also a useful reagent for investigating the structure/activity relationships of non-nucleoside adenosine kinase inhibitors.

Synthesis

General procedure for the synthesis of 2-bromo-5-iodopyridine from 2-amino-5-iodopyridine: Bromine (3 mL) was slowly added dropwise to a mixture of 2-amino-5-iodopyridine (5 g, 20 mmol) dissolved in 48% aqueous hydrobromic acid (10 mL), and the reaction system was cooled by an ice bath to maintain the reaction at low temperature. Subsequently, sodium nitrite (3.4 g, dissolved in 5 mL of water) solution was added dropwise, and the reaction temperature was controlled not to exceed 15 °C. After the dropwise addition, a solution of sodium hydroxide (16 g) in water (40 mL) was added. A brown solid precipitated from the reaction mixture and was extracted with dichloromethane (50 mL). The organic phases were combined, washed sequentially with water and saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to afford the target product 2-bromo-5-iodopyridine (4.4 g, 78% yield).

References

[1] Journal of Heterocyclic Chemistry, 2017, vol. 54, # 5, p. 2656 - 2663
[2] Journal of Organic Chemistry, 2009, vol. 74, # 15, p. 5228 - 5236
[3] Bioorganic and Medicinal Chemistry, 1999, vol. 7, # 3, p. 467 - 479
[4] Patent: WO2005/92304, 2005, A2. Location in patent: Page/Page column 42
[5] Tetrahedron, 2002, vol. 58, # 14, p. 2885 - 2890

2-Bromo-5-iodopyridine(73290-22-9)Related Product Information

• 3-Bromoanisole
• 2-Bromo-5-chloropyridine
• 2,6-Lutidine
• 2-Bromo-5-fluoropyridine
• 1-Hexadecylpyridinium bromide
• 2-Bromopyridine
• 2-Hydroxypyridine
• Sulfasalazine
• Chromium picolinate
• 2-BROMO-5-IODOBENZONITRILE
• Bromine
• 2-BROMO-3,5-DIIODOPYRIDINE
• 2-BROMO-5-IODO-4-METHYLPYRIDINE
• 2-BROMO-5-IODO-3-METHYLPYRIDINE
• 4-BROMO-2-IODOPYRIDINE
• 4-AMINO-3-BROMO-5-IODOPYRIDINE
• 3-BROMO-2-IODOPYRIDINE
• 2-Amino-3-bromo-5-iodopyridine