(5-Amino-6-chloropyridin-3-yl)boronic acid
95%
- Product Code: 37041
CAS:
1354697-94-1
| Molecular Weight: | 172.3773 g./mol | Molecular Formula: | C₅H₆BClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13189112 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(5-Amino-6-chloropyridin-3-yl)boronic acid is primarily utilized in organic synthesis as a key intermediate in the preparation of various pharmaceuticals and biologically active compounds. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This makes it valuable in the development of complex molecules, particularly in drug discovery and medicinal chemistry. Additionally, it serves as a building block for creating ligands and catalysts used in asymmetric synthesis. Its unique structure also allows for potential applications in the design of enzyme inhibitors and other therapeutic agents targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,584.00 |
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(5-Amino-6-chloropyridin-3-yl)boronic acid
(5-Amino-6-chloropyridin-3-yl)boronic acid is primarily utilized in organic synthesis as a key intermediate in the preparation of various pharmaceuticals and biologically active compounds. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This makes it valuable in the development of complex molecules, particularly in drug discovery and medicinal chemistry. Additionally, it serves as a building block for creating ligands and catalysts used in asymmetric synthesis. Its unique structure also allows for potential applications in the design of enzyme inhibitors and other therapeutic agents targeting specific biological pathways.
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