1-Tosyl-7-azaindole-3-boronic Acid Pinacol Ester
≥95%
- Product Code: 89497
CAS:
866545-91-7
| Molecular Weight: | 398.28 g./mol | Molecular Formula: | C₂₀H₂₃N₂O₄SB |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11616456 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic ester group enables efficient formation of carbon-carbon bonds, making it valuable for creating diverse heterocyclic compounds. Additionally, it is employed in the synthesis of biologically active molecules, including potential drug candidates, due to its ability to introduce the azaindole moiety, which is often found in compounds with therapeutic properties. Its tosyl group further enhances its reactivity and selectivity in various chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,890.00 |
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| 0.250 | 10-20 days | ฿4,500.00 |
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| 1.000 | 10-20 days | ฿16,200.00 |
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1-Tosyl-7-azaindole-3-boronic Acid Pinacol Ester
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic ester group enables efficient formation of carbon-carbon bonds, making it valuable for creating diverse heterocyclic compounds. Additionally, it is employed in the synthesis of biologically active molecules, including potential drug candidates, due to its ability to introduce the azaindole moiety, which is often found in compounds with therapeutic properties. Its tosyl group further enhances its reactivity and selectivity in various chemical transformations.
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