Methyl 2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
98%
- Product Code: 66919
CAS:
1073371-99-9
| Molecular Weight: | 278.11 g./mol | Molecular Formula: | C₁₄H₁₉BO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08458200 | |
| Melting Point: | Boiling Point: | 383.9±32.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the construction of complex organic molecules, particularly in pharmaceutical and materials science research. The compound’s structure allows it to act as a coupling partner for aryl halides, enabling the formation of biaryl structures, which are common in drug molecules and advanced materials. Additionally, its ester group provides further reactivity for derivatization, making it a useful building block in the development of fine chemicals and specialized polymers. Its stability and compatibility with various reaction conditions enhance its utility in synthetic chemistry workflows.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,862.00 |
+
-
|
| 0.250 | 10-20 days | ฿3,447.00 |
+
-
|
| 1.000 | 10-20 days | ฿7,677.00 |
+
-
|
| 5.000 | 10-20 days | ฿25,110.00 |
+
-
|
Methyl 2-hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
This chemical is primarily utilized in organic synthesis as a versatile intermediate. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the construction of complex organic molecules, particularly in pharmaceutical and materials science research. The compound’s structure allows it to act as a coupling partner for aryl halides, enabling the formation of biaryl structures, which are common in drug molecules and advanced materials. Additionally, its ester group provides further reactivity for derivatization, making it a useful building block in the development of fine chemicals and specialized polymers. Its stability and compatibility with various reaction conditions enhance its utility in synthetic chemistry workflows.
| 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:
฿0.00
฿0.00
Total :