(5-((4-(tert-Butoxycarbonyl)piperazin-1-yl) sulfonyl)-2-methoxyphenyl)boronic acid
98%
- Product Code: 89330
CAS:
1704095-62-4
Molecular Weight: | 400.25 g./mol | Molecular Formula: | C₁₆H₂₅BN₂O₇S |
---|---|---|---|
EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceutical compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex molecules, including drug candidates. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety ensures selective reactivity during multi-step synthetic processes, allowing for the controlled introduction of functional groups. Additionally, the methoxy and sulfonyl groups contribute to its versatility in designing molecules with specific biological activities, particularly in the development of enzyme inhibitors or receptor modulators. Its applications are often seen in the synthesis of compounds targeting diseases such as cancer, neurological disorders, and infectious diseases.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
0.500 | 10-20 days | ฿29,840.00 |
+
-
|
(5-((4-(tert-Butoxycarbonyl)piperazin-1-yl) sulfonyl)-2-methoxyphenyl)boronic acid
This chemical is primarily used in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceutical compounds. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex molecules, including drug candidates. The tert-butoxycarbonyl (Boc) protecting group on the piperazine moiety ensures selective reactivity during multi-step synthetic processes, allowing for the controlled introduction of functional groups. Additionally, the methoxy and sulfonyl groups contribute to its versatility in designing molecules with specific biological activities, particularly in the development of enzyme inhibitors or receptor modulators. Its applications are often seen in the synthesis of compounds targeting diseases such as cancer, neurological disorders, and infectious diseases.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Cart
No products
Subtotal:
฿0.00
฿0.00
Total :