1H-indazol-4-yl-4-boronic acid
98%
- Product Code: 89528
CAS:
1023595-17-6
| Molecular Weight: | 161.96 g./mol | Molecular Formula: | C₇H₇BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09878901 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃ |
Product Description:
1H-indazol-4-yl-4-boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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, including potential drug candidates. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the creation of diverse organic structures. Additionally, it is utilized in research and development for exploring new chemical entities and optimizing synthetic routes in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,410.00 |
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1H-indazol-4-yl-4-boronic acid
1H-indazol-4-yl-4-boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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, including potential drug candidates. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the creation of diverse organic structures. Additionally, it is utilized in research and development for exploring new chemical entities and optimizing synthetic routes in medicinal chemistry.
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