2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene
98%
- Product Code: 242285
CAS:
853377-11-4
| Molecular Weight: | Molecular Formula: | C₂₂H₂₁BO₂ | |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11977261 | |
| Melting Point: | 128 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature |
Product Description:
Used primarily in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the construction of complex aromatic and conjugated systems. Its pyrene core provides a rigid, planar structure that enhances π-π stacking interactions, making it valuable in the development of organic semiconductors, fluorescent sensors, and optoelectronic materials such as OLEDs and organic field-effect transistors (OFETs). The boronate ester group offers high stability and reactivity under mild conditions, facilitating efficient coupling with aryl halides. It is also employed in the synthesis of polycyclic aromatic hydrocarbons (PAHs) and molecular probes for imaging and sensing applications due to its strong fluorescence and environmental sensitivity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £95.18 |
+
-
|
| 1.000 | 10-20 days | £254.11 |
+
-
|
| 5.000 | 10-20 days | £914.80 |
+
-
|
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene
Used primarily in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the construction of complex aromatic and conjugated systems. Its pyrene core provides a rigid, planar structure that enhances π-π stacking interactions, making it valuable in the development of organic semiconductors, fluorescent sensors, and optoelectronic materials such as OLEDs and organic field-effect transistors (OFETs). The boronate ester group offers high stability and reactivity under mild conditions, facilitating efficient coupling with aryl halides. It is also employed in the synthesis of polycyclic aromatic hydrocarbons (PAHs) and molecular probes for imaging and sensing applications due to its strong fluorescence and environmental sensitivity.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
£0.00
£0.00
Total :