2-Bromoiodobenzene
98%, with stabilizer copper shavings
- Product Code: 123261
Alias:
o-bromoiodobenzene; 1-bromo-2-iodobenzene, 2-iodobenzonitrile
CAS:
583-55-1
| Molecular Weight: | 282.9 g./mol | Molecular Formula: | BrC₆H₄I |
|---|---|---|---|
| EC Number: | 209-508-9 | MDL Number: | MFCD00001030 |
| Melting Point: | 9-10 °C(lit.) | Boiling Point: | 120-121 °C15 mm Hg(lit.) |
| Density: | 2.203 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
2-Bromoiodobenzene is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. It is commonly employed in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to form carbon-carbon bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its dual halogen functionality allows for selective reactivity, enabling chemists to introduce specific structural motifs into target compounds. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds and functionalized aromatic systems, which are valuable in drug discovery and material science. Its stability and reactivity make it a useful reagent in both academic research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98-100 |
| Refractive Index N20/D | 1.6625-1.6675 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
| Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $12.04 |
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| 5.000 | 10-20 days | $17.03 |
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| 25.000 | 10-20 days | $27.41 |
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| 100.000 | 10-20 days | $107.98 |
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| 500.000 | 10-20 days | $534.89 |
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2-Bromoiodobenzene
2-Bromoiodobenzene is primarily utilized in organic synthesis as a versatile intermediate for constructing complex molecules. It is commonly employed in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to form carbon-carbon bonds, which are essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its dual halogen functionality allows for selective reactivity, enabling chemists to introduce specific structural motifs into target compounds. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds and functionalized aromatic systems, which are valuable in drug discovery and material science. Its stability and reactivity make it a useful reagent in both academic research and industrial applications.
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