4,4,5,5-Tetramethyl-2-(naphthalen-1-ylmethyl)-1,3,2-dioxaborolane
≥95%
- Product Code: 90303
CAS:
475250-57-8
| Molecular Weight: | 268.16 g./mol | Molecular Formula: | C₁₇H₂₁BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22419278 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This process is widely applied in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable tool in the development of new compounds, especially in medicinal chemistry for drug discovery and development. Additionally, it is used in the preparation of functionalized polymers and materials for electronic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $93.12 |
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4,4,5,5-Tetramethyl-2-(naphthalen-1-ylmethyl)-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This process is widely applied in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a valuable tool in the development of new compounds, especially in medicinal chemistry for drug discovery and development. Additionally, it is used in the preparation of functionalized polymers and materials for electronic applications.
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