(3-Chloro-4-((4-ethylpiperazin-1-yl)methyl)phenyl)boronic acid
98%
- Product Code: 89127
CAS:
1704074-25-8
| Molecular Weight: | 282.58 g./mol | Molecular Formula: | C₁₃H₂₀BClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400363 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical and materials science industries. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex organic molecules, including drug candidates and advanced materials. Additionally, the presence of the ethylpiperazine moiety enhances its solubility and reactivity in various reaction conditions, making it a versatile intermediate in medicinal chemistry for the development of biologically active compounds. Its applications also extend to the synthesis of polymers and other specialty chemicals where precise molecular architecture is required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿33,930.00 |
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(3-Chloro-4-((4-ethylpiperazin-1-yl)methyl)phenyl)boronic acid
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical and materials science industries. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex organic molecules, including drug candidates and advanced materials. Additionally, the presence of the ethylpiperazine moiety enhances its solubility and reactivity in various reaction conditions, making it a versatile intermediate in medicinal chemistry for the development of biologically active compounds. Its applications also extend to the synthesis of polymers and other specialty chemicals where precise molecular architecture is required.
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