(4-(2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)ethoxy)-3-chlorophenyl)boronic acid
98%
- Product Code: 89234
CAS:
1704074-18-9
| Molecular Weight: | 384.67 g./mol | Molecular Formula: | C₁₇H₂₆BClN₂O₅ |
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| EC Number: | MDL Number: | MFCD28400359 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate in the development of biologically active compounds. Its structure, featuring a boronic acid group and a piperazine moiety, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it is often used in the preparation of potential drug candidates, particularly in the design of molecules targeting central nervous system disorders, due to the presence of the piperazine group, which is a common pharmacophore in medicinal chemistry. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | €1,037.60 |
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(4-(2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)ethoxy)-3-chlorophenyl)boronic acid
This chemical is primarily utilized in organic synthesis and pharmaceutical research as a key intermediate in the development of biologically active compounds. Its structure, featuring a boronic acid group and a piperazine moiety, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it is often used in the preparation of potential drug candidates, particularly in the design of molecules targeting central nervous system disorders, due to the presence of the piperazine group, which is a common pharmacophore in medicinal chemistry. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling further functionalization in multi-step synthetic processes.
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