- 2-Bromo-5-iodopyridine
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- $1.10
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2026-08-20
- CAS:73290-22-9
- Min. Order: 1g
- Purity: 99.00%
- Supply Ability: 100 Tons min
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| | 2-Bromo-5-iodopyridine Basic information |
| | 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) |
| Hazard Codes | Xn,Xi | | Risk Statements | 22-37/38-41 | | Safety Statements | 26-36/39 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29333990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3 |
| | 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 Preparation Products And Raw materials |
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