(N-Boc-5-bromo-2-indolyl)boronic acid
95%
- Product Code: 91011
Alias:
N-Boc-5-bromoindole-2-boronic acid
1-(tert-butoxycarbonyl-5-bromo-1H-indol-2-yl)boronic acid
CAS:
475102-13-7
| Molecular Weight: | 339.98 g./mol | Molecular Formula: | C₁₃H₁₅BBrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03701683 | |
| Melting Point: | 93 °C | Boiling Point: | |
| Density: | 1.45 | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the preparation of complex indole derivatives, which are important in pharmaceutical research and drug development. The N-Boc protecting group ensures stability during reactions, while the boronic acid moiety facilitates coupling with aryl or vinyl halides. Its application extends to the synthesis of biologically active compounds, including potential anticancer and anti-inflammatory agents. The bromo substituent on the indole ring allows for further functionalization, making it a versatile building block in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 95 100% |
| APPEARANCE | WHITE TO LIGHT BROWN POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,050.00 |
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| 5.000 | 10-20 days | ฿4,050.00 |
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(N-Boc-5-bromo-2-indolyl)boronic acid
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the preparation of complex indole derivatives, which are important in pharmaceutical research and drug development. The N-Boc protecting group ensures stability during reactions, while the boronic acid moiety facilitates coupling with aryl or vinyl halides. Its application extends to the synthesis of biologically active compounds, including potential anticancer and anti-inflammatory agents. The bromo substituent on the indole ring allows for further functionalization, making it a versatile building block in medicinal chemistry.
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