2-(1,3-Dioxolan-2-yl)]ethyl]zinc bromide solution
0.5 M in THF
- Product Code: 77830
CAS:
307531-83-5
| Molecular Weight: | 246.42 g./mol | Molecular Formula: | C₅H₉BrO₂Zn |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02260129 | |
| Melting Point: | Boiling Point: | 65℃ | |
| Density: | 0.984 g/mL at 25℃ | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily used in organic synthesis as a reagent for introducing the 2-(1,3-dioxolan-2-yl)ethyl group into various organic molecules. It is particularly valuable in the formation of carbon-carbon bonds, making it useful in the synthesis of complex organic compounds. The dioxolane group in the reagent can act as a protecting group for carbonyl compounds, allowing selective reactions to occur at other sites within the molecule. This reagent is often employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over molecular structure is critical. Its application in organozinc chemistry also makes it a key component in cross-coupling reactions, such as Negishi coupling, which is widely used in the construction of carbon frameworks in organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 50.000 | 10-20 days | ฿26,532.00 |
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2-(1,3-Dioxolan-2-yl)]ethyl]zinc bromide solution
This chemical is primarily used in organic synthesis as a reagent for introducing the 2-(1,3-dioxolan-2-yl)ethyl group into various organic molecules. It is particularly valuable in the formation of carbon-carbon bonds, making it useful in the synthesis of complex organic compounds. The dioxolane group in the reagent can act as a protecting group for carbonyl compounds, allowing selective reactions to occur at other sites within the molecule. This reagent is often employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over molecular structure is critical. Its application in organozinc chemistry also makes it a key component in cross-coupling reactions, such as Negishi coupling, which is widely used in the construction of carbon frameworks in organic chemistry.
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