4,4,5,5-Tetramethyl-2-(3-phenoxyphenyl)-1,3,2-dioxaborolane
≥95%
- Product Code: 118369
CAS:
864772-18-9
| Molecular Weight: | 296.17 g./mol | Molecular Formula: | C₁₈H₂₁BO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11973622 | |
| Melting Point: | Boiling Point: | 402.8±28.0°C at 760 mmHg | |
| Density: | 1.09g/cm3 | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis as a versatile intermediate, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure enhances stability and reactivity, enabling efficient coupling with aryl halides. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to create complex aromatic structures. Its application in medicinal chemistry includes the synthesis of bioactive compounds and drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,358.00 |
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| 0.250 | 10-20 days | ฿3,528.00 |
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| 1.000 | 10-20 days | ฿8,802.00 |
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4,4,5,5-Tetramethyl-2-(3-phenoxyphenyl)-1,3,2-dioxaborolane
This chemical is primarily used in organic synthesis as a versatile intermediate, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure enhances stability and reactivity, enabling efficient coupling with aryl halides. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to create complex aromatic structures. Its application in medicinal chemistry includes the synthesis of bioactive compounds and drug candidates.
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