6-Amino-5-fluoropyridine-3-boronic Acid Pinacol Ester
95%
- Product Code: 90166
CAS:
944401-75-6
| Molecular Weight: | 238.07 g./mol | Molecular Formula: | C₁₁H₁₆BFN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12923417 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in Suzuki-Miyaura cross-coupling reactions, a widely employed method in organic synthesis for forming carbon-carbon bonds. Its boronic ester group enables it to act as a key reagent in coupling with aryl or vinyl halides, facilitating the creation of complex biaryl structures. These structures are essential in the development of pharmaceuticals, agrochemicals, and organic materials. Its fluoropyridine moiety further enhances its reactivity and selectivity, making it valuable in the synthesis of biologically active molecules, particularly in drug discovery and development. Additionally, it is used in the preparation of advanced materials, such as organic electronics and liquid crystals, due to its ability to introduce fluorine atoms into target molecules, which can modify their electronic properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,352.00 |
+
-
|
| 0.250 | 10-20 days | ฿14,220.00 |
+
-
|
| 1.000 | 10-20 days | ฿34,020.00 |
+
-
|
6-Amino-5-fluoropyridine-3-boronic Acid Pinacol Ester
This compound is primarily utilized in Suzuki-Miyaura cross-coupling reactions, a widely employed method in organic synthesis for forming carbon-carbon bonds. Its boronic ester group enables it to act as a key reagent in coupling with aryl or vinyl halides, facilitating the creation of complex biaryl structures. These structures are essential in the development of pharmaceuticals, agrochemicals, and organic materials. Its fluoropyridine moiety further enhances its reactivity and selectivity, making it valuable in the synthesis of biologically active molecules, particularly in drug discovery and development. Additionally, it is used in the preparation of advanced materials, such as organic electronics and liquid crystals, due to its ability to introduce fluorine atoms into target molecules, which can modify their 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:
฿0.00
฿0.00
Total :