N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acrylamide
98%
- Product Code: 91018
CAS:
874363-18-5
| Molecular Weight: | 273.14 g./mol | Molecular Formula: | C₁₅H₂₀BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22493996 | |
| Melting Point: | 160℃ | Boiling Point: | |
| Density: | Storage Condition: | 2-8℃, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the field of polymer chemistry and materials science. It serves as a key monomer in the production of advanced polymeric materials, enabling the incorporation of boronate ester functionalities into polymer chains. These functionalities are valuable for creating stimuli-responsive materials, such as those that react to changes in pH, glucose levels, or other biological conditions, making it useful in biomedical applications like drug delivery systems and biosensors. Additionally, its acrylamide group allows for polymerization via radical mechanisms, facilitating the development of hydrogels and other cross-linked networks. The compound is also employed in the synthesis of organic electronic materials, where its boronate ester group can participate in cross-coupling reactions, contributing to the fabrication of conjugated polymers for optoelectronic devices.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,430.00 |
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N-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acrylamide
This chemical is primarily utilized in organic synthesis, particularly in the field of polymer chemistry and materials science. It serves as a key monomer in the production of advanced polymeric materials, enabling the incorporation of boronate ester functionalities into polymer chains. These functionalities are valuable for creating stimuli-responsive materials, such as those that react to changes in pH, glucose levels, or other biological conditions, making it useful in biomedical applications like drug delivery systems and biosensors. Additionally, its acrylamide group allows for polymerization via radical mechanisms, facilitating the development of hydrogels and other cross-linked networks. The compound is also employed in the synthesis of organic electronic materials, where its boronate ester group can participate in cross-coupling reactions, contributing to the fabrication of conjugated polymers for optoelectronic devices.
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