2-Chloro-5-(trifluoromethyl)benzeneboronic acid
96%
- Product Code: 89784
Alias:
2-Chloro-5-(trifluoromethyl)phenylboronic acid
CAS:
182344-18-9
| Molecular Weight: | 224.37 g./mol | Molecular Formula: | C₇H₅BClF₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00797335 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
2-Chloro-5-(trifluoromethyl)benzeneboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex molecules, especially those containing trifluoromethyl groups, which are known for their stability and bioactivity. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse organic compounds. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) and fine chemicals, where precise molecular structures are critical. Its unique properties make it a versatile reagent in medicinal chemistry and material science research.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96-100 |
| APPEARANCE | White to tan solid |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $22.43 |
+
-
|
| 5.000 | 10-20 days | $78.07 |
+
-
|
2-Chloro-5-(trifluoromethyl)benzeneboronic acid
2-Chloro-5-(trifluoromethyl)benzeneboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex molecules, especially those containing trifluoromethyl groups, which are known for their stability and bioactivity. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse organic compounds. Additionally, it is employed in the development of active pharmaceutical ingredients (APIs) and fine chemicals, where precise molecular structures are critical. Its unique properties make it a versatile reagent in medicinal chemistry and material science research.
| 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 :