2-(Diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
≥98%(GC)(T)
- Product Code: 73912
CAS:
2066512-27-2
| Molecular Weight: | 393.8 g./mol | Molecular Formula: | C₇H₁₃BI₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31690012 | |
| Melting Point: | 80 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8 ℃, inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a key reagent for introducing diiodomethyl groups into various molecular frameworks. It is particularly valuable in the preparation of complex organic compounds, where it serves as a versatile building block. The compound is often employed in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, its unique structure makes it useful in the synthesis of boron-containing compounds, which have applications in materials science, including the development of advanced polymers and optoelectronic materials. Its stability and reactivity under mild conditions make it a preferred choice in laboratories for constructing intricate molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,872.00 |
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2-(Diiodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis as a key reagent for introducing diiodomethyl groups into various molecular frameworks. It is particularly valuable in the preparation of complex organic compounds, where it serves as a versatile building block. The compound is often employed in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, its unique structure makes it useful in the synthesis of boron-containing compounds, which have applications in materials science, including the development of advanced polymers and optoelectronic materials. Its stability and reactivity under mild conditions make it a preferred choice in laboratories for constructing intricate molecular architectures.
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