(4-((2-Acrylamidoethyl)carbamoyl)-3-fluorophenyl)boronic acid
95%
- Product Code: 89178
CAS:
1313712-90-1
| Molecular Weight: | 280.06 g./mol | Molecular Formula: | C₁₂H₁₄BFN₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32856191 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8 ℃, inert gas storage |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its boronic acid functional group, which is known for its ability to form stable covalent bonds with diols and other nucleophiles. It is often employed in the development of boron-containing drugs, particularly in the synthesis of protease inhibitors and other therapeutic agents targeting specific enzymes. Additionally, its acrylamide moiety makes it suitable for polymerization reactions, enabling its use in the creation of advanced materials such as hydrogels or molecularly imprinted polymers. These materials have applications in drug delivery systems, biosensors, and separation technologies. The fluorine atom in its structure can enhance binding affinity and metabolic stability, making it valuable in the design of bioactive molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,630.00 |
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| 0.250 | 10-20 days | ฿11,460.00 |
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| 1.000 | 10-20 days | ฿27,960.00 |
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(4-((2-Acrylamidoethyl)carbamoyl)-3-fluorophenyl)boronic acid
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its boronic acid functional group, which is known for its ability to form stable covalent bonds with diols and other nucleophiles. It is often employed in the development of boron-containing drugs, particularly in the synthesis of protease inhibitors and other therapeutic agents targeting specific enzymes. Additionally, its acrylamide moiety makes it suitable for polymerization reactions, enabling its use in the creation of advanced materials such as hydrogels or molecularly imprinted polymers. These materials have applications in drug delivery systems, biosensors, and separation technologies. The fluorine atom in its structure can enhance binding affinity and metabolic stability, making it valuable in the design of bioactive molecules.
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