2-(4-(tert-Butoxycarbonyl)piperazin-1-ylsulfonyl)phenylboronic acid
98%
- Product Code: 89626
CAS:
1704063-63-7
| Molecular Weight: | 370.24 g./mol | Molecular Formula: | C₁₅H₂₃BN₂O₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28396568 | |
| 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. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds, enabling the construction of complex organic molecules. Its piperazine moiety, protected by a tert-butoxycarbonyl (Boc) group, allows for selective deprotection and functionalization, making it useful in the development of pharmaceuticals and biologically active compounds. Additionally, the sulfonyl group enhances its reactivity and stability, facilitating its use in designing drug candidates and fine chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿50,200.00 |
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2-(4-(tert-Butoxycarbonyl)piperazin-1-ylsulfonyl)phenylboronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form carbon-carbon bonds, enabling the construction of complex organic molecules. Its piperazine moiety, protected by a tert-butoxycarbonyl (Boc) group, allows for selective deprotection and functionalization, making it useful in the development of pharmaceuticals and biologically active compounds. Additionally, the sulfonyl group enhances its reactivity and stability, facilitating its use in designing drug candidates and fine chemicals.
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