Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthoate
95%
- Product Code: 46600
CAS:
643094-08-0
| Molecular Weight: | 312.1680 g./mol | Molecular Formula: | C₁₈H₂₁BO₄ |
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| EC Number: | MDL Number: | MFCD17015822 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic electronic materials, including OLEDs and semiconductors, due to its ability to facilitate precise molecular design and functionalization. Its stability and reactivity under mild conditions make it a versatile tool in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $100.92 |
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Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthoate
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex organic molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of organic electronic materials, including OLEDs and semiconductors, due to its ability to facilitate precise molecular design and functionalization. Its stability and reactivity under mild conditions make it a versatile tool in synthetic chemistry.
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