1-Bromo-3-iodopropane
98%,stabilizedwithCopperchip
- Product Code: 40030
CAS:
22306-36-1
| Molecular Weight: | 248.8882 g./mol | Molecular Formula: | C₃H₆BrI |
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| Density: | Storage Condition: | room temperature |
Product Description:
1-Bromo-3-iodopropane is primarily used as a versatile intermediate in organic synthesis. It is often employed in the preparation of various organic compounds, particularly in the formation of complex molecules through nucleophilic substitution reactions. The compound is valuable in the synthesis of pharmaceuticals, where it serves as a building block for active pharmaceutical ingredients (APIs). Additionally, it is utilized in the development of agrochemicals, contributing to the creation of pesticides and herbicides. In material science, 1-bromo-3-iodopropane is used in the modification of polymers and the synthesis of specialty chemicals. Its dual halogen functionality allows for selective reactivity, making it a useful reagent in cross-coupling reactions, such as those involving palladium-catalyzed processes. This compound is also applied in research laboratories for studying reaction mechanisms and developing new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft11,151.20 |
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1-Bromo-3-iodopropane
1-Bromo-3-iodopropane is primarily used as a versatile intermediate in organic synthesis. It is often employed in the preparation of various organic compounds, particularly in the formation of complex molecules through nucleophilic substitution reactions. The compound is valuable in the synthesis of pharmaceuticals, where it serves as a building block for active pharmaceutical ingredients (APIs). Additionally, it is utilized in the development of agrochemicals, contributing to the creation of pesticides and herbicides. In material science, 1-bromo-3-iodopropane is used in the modification of polymers and the synthesis of specialty chemicals. Its dual halogen functionality allows for selective reactivity, making it a useful reagent in cross-coupling reactions, such as those involving palladium-catalyzed processes. This compound is also applied in research laboratories for studying reaction mechanisms and developing new synthetic methodologies.
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