2-(2-Fluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 41341
CAS:
1377152-43-6
| Molecular Weight: | 248.1009 g./mol | Molecular Formula: | C₁₄H₁₈BFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19703878 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorinated styryl moiety can enhance the stability and reactivity of the compound, enabling its use in the development of fluorescent probes and imaging agents for biological research. Its unique structure also makes it suitable for applications in material science, such as in the synthesis of organic electronic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿7,659.00 |
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2-(2-Fluorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorinated styryl moiety can enhance the stability and reactivity of the compound, enabling its use in the development of fluorescent probes and imaging agents for biological research. Its unique structure also makes it suitable for applications in material science, such as in the synthesis of organic electronic materials.
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