4-Iodobenzyl bromide
97%
- Product Code: 119560
Alias:
p-Iodobenzyl bromide; 4-iodobenzyl bromide
CAS:
16004-15-2
| Molecular Weight: | 296.93 g./mol | Molecular Formula: | C₇H₆BrI |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00209656 | |
| Melting Point: | 78-82 °C(lit.) | Boiling Point: | 140°C 15mm |
| Density: | Storage Condition: | 2~8°C, away from light |
Product Description:
Used primarily as a reagent in organic synthesis, 4-Iodobenzyl bromide is valuable for introducing the 4-iodobenzyl group into molecules. It is commonly employed in the preparation of pharmaceuticals, particularly in the synthesis of complex organic compounds. The compound is also utilized in the development of materials for organic electronics, where it acts as a building block for creating functionalized aromatic systems. Additionally, it finds application in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for constructing carbon-carbon bonds in advanced chemical research.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 78 Degree Celsius-82 Degree Celsius |
| Purity (GC) | 96.5%-100% |
| Purity (Titration By AgNO3 After O2 Combustion) | 96.5%-103.5% |
| Purity (Titration By AgNO3 After O2 Combustion) | 96.5%-103.5% |
| Appearance | White To Beige Powder Or Crystals |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft4,094.16 |
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| 5.000 | 10-20 days | Ft13,036.67 |
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| 25.000 | 10-20 days | Ft60,335.00 |
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| 100.000 | 10-20 days | Ft217,206.02 |
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4-Iodobenzyl bromide
Used primarily as a reagent in organic synthesis, 4-Iodobenzyl bromide is valuable for introducing the 4-iodobenzyl group into molecules. It is commonly employed in the preparation of pharmaceuticals, particularly in the synthesis of complex organic compounds. The compound is also utilized in the development of materials for organic electronics, where it acts as a building block for creating functionalized aromatic systems. Additionally, it finds application in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for constructing carbon-carbon bonds in advanced chemical research.
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