4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
98%
- Product Code: 90742
CAS:
171364-82-2
| Molecular Weight: | 229.0800 g./mol | Molecular Formula: | C₁₃H₁₆BNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03093897 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Additionally, it serves as a precursor in the development of liquid crystals and organic light-emitting diodes (OLEDs), contributing to advancements in display technologies. Its nitrile group also allows for further functionalization, making it versatile in the synthesis of various bioactive compounds and polymers.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 97.5 100% |
| Melting point | 94 99? |
| Appearance | White to Tan to Very Dark Orange Powder, Crystals or Crystalline Powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $15.78 |
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| 5.000 | 10-20 days | $64.79 |
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| 25.000 | 10-20 days | $282.40 |
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| 100.000 | 10-20 days | $797.36 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Additionally, it serves as a precursor in the development of liquid crystals and organic light-emitting diodes (OLEDs), contributing to advancements in display technologies. Its nitrile group also allows for further functionalization, making it versatile in the synthesis of various bioactive compounds and polymers.
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