1,4-Benzenediboronic Acid Bis(pinacol) Ester
97%
- Product Code: 89439
CAS:
99770-93-1
| Molecular Weight: | Molecular Formula: | C₁₈H₂₈B₂O₄ | |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08276852 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
1,4-Benzenedibiboronic acid bis(pinacol) ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for creating biaryl compounds, which are common in drug development and organic electronics. Additionally, it is utilized in the preparation of polymers and functional materials due to its ability to introduce boronic ester groups into molecular structures.
Product Specification:
| Test | Specification |
|---|---|
| PURITYT | 96.5 100% |
| Melting point | 241 246? |
| Appearance | White to light yellow crystalline solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €13.19 |
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| 5.000 | 10-20 days | €45.38 |
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| 25.000 | 10-20 days | €157.76 |
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| 100.000 | 10-20 days | €507.85 |
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1,4-Benzenediboronic Acid Bis(pinacol) Ester
1,4-Benzenedibiboronic acid bis(pinacol) ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for creating biaryl compounds, which are common in drug development and organic electronics. Additionally, it is utilized in the preparation of polymers and functional materials due to its ability to introduce boronic ester groups into molecular structures.
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