(3-((tert-Butoxycarbonyl)amino) -4-fluorophenyl)boronic acid
98%
- Product Code: 65446
CAS:
1704069-72-6
| Molecular Weight: | 255.06 g./mol | Molecular Formula: | C₁₁H₁₅BFNO₄ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, enabling the formation of carbon-carbon bonds with high precision. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in constructing complex organic molecules. Additionally, the tert-butoxycarbonyl (Boc) protecting group on the amino functionality allows for selective deprotection, enabling further modifications in multi-step synthetic processes. This compound is especially useful in medicinal chemistry for developing drug candidates and bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $2,085.17 |
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(3-((tert-Butoxycarbonyl)amino) -4-fluorophenyl)boronic acid
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of pharmaceuticals, enabling the formation of carbon-carbon bonds with high precision. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in constructing complex organic molecules. Additionally, the tert-butoxycarbonyl (Boc) protecting group on the amino functionality allows for selective deprotection, enabling further modifications in multi-step synthetic processes. This compound is especially useful in medicinal chemistry for developing drug candidates and bioactive molecules.
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