(4-Chloro-3-(4-oxopiperidine-1-carbonyl)phenyl)boronic acid
98%
- Product Code: 89305
CAS:
1704080-21-6
| Molecular Weight: | 281.51 g./mol | Molecular Formula: | C₁₂H₁₃BClNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400397 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it serves as a boronic acid reagent. Its structure, featuring a boronic acid group, makes it effective for forming carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The compound is also used in the development of bioactive compounds and materials science research, where its unique functional groups allow for precise modifications in molecular design. Additionally, it finds applications in the preparation of intermediates for drug discovery, particularly in creating compounds with potential therapeutic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $5,166.04 |
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(4-Chloro-3-(4-oxopiperidine-1-carbonyl)phenyl)boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it serves as a boronic acid reagent. Its structure, featuring a boronic acid group, makes it effective for forming carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The compound is also used in the development of bioactive compounds and materials science research, where its unique functional groups allow for precise modifications in molecular design. Additionally, it finds applications in the preparation of intermediates for drug discovery, particularly in creating compounds with potential therapeutic properties.
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