4,4,5,5-Tetramethyl-2-(3-((2,2,2-trifluoroethyl)thio)phenyl)-1,3,2-dioxaborolane
97%
- Product Code: 118373
CAS:
1026797-07-8
| Molecular Weight: | 318.16 g./mol | Molecular Formula: | C₁₄H₁₈BF₃O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11520054 | |
| Melting Point: | Boiling Point: | 354.1±42.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling of aromatic rings is required. Additionally, it finds use in materials science for the development of organic electronic materials, where its stability and reactivity are advantageous. Its trifluoroethylthio group further enhances its utility in creating compounds with unique electronic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft41,114.00 |
+
-
|
| 0.250 | 10-20 days | Ft81,937.09 |
+
-
|
| 1.000 | 10-20 days | Ft221,472.56 |
+
-
|
| 5.000 | 10-20 days | Ft652,587.72 |
+
-
|
4,4,5,5-Tetramethyl-2-(3-((2,2,2-trifluoroethyl)thio)phenyl)-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the pharmaceutical industry for the synthesis of drug intermediates, where precise and efficient coupling of aromatic rings is required. Additionally, it finds use in materials science for the development of organic electronic materials, where its stability and reactivity are advantageous. Its trifluoroethylthio group further enhances its utility in creating compounds with unique electronic properties.
| 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 | - |
Cart
No products
Subtotal:
Ft0.00
Ft0.00
Total :