(3-((4-(tert-Butoxycarbonyl)piperazin-1-yl)sulfonyl)-4-methoxyphenyl)boronic acid
98%
- Product Code: 65430
CAS:
1704081-10-6
| Molecular Weight: | 400.26 g./mol | Molecular Formula: | C₁₆H₂₅BN₂O₇S |
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| EC Number: | MDL Number: | MFCD28805555 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceuticals. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds in the synthesis of complex organic molecules, including drug candidates. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection, enabling further functionalization of the molecule. It is particularly relevant in the design and synthesis of protease inhibitors and other biologically active compounds targeting various diseases. Additionally, its sulfonyl group enhances its reactivity and stability, making it suitable for use in combinatorial chemistry and high-throughput screening processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿42,100.00 |
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(3-((4-(tert-Butoxycarbonyl)piperazin-1-yl)sulfonyl)-4-methoxyphenyl)boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceuticals. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to form carbon-carbon bonds in the synthesis of complex organic molecules, including drug candidates. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety allows for selective deprotection, enabling further functionalization of the molecule. It is particularly relevant in the design and synthesis of protease inhibitors and other biologically active compounds targeting various diseases. Additionally, its sulfonyl group enhances its reactivity and stability, making it suitable for use in combinatorial chemistry and high-throughput screening processes.
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