4-(tert-Butoxycarbonyl)benzeneboronic acid
98%
- Product Code: 60832
Alias:
4-(tert-butoxycarbonyl)phenylboronic acid
CAS:
850568-54-6
| Molecular Weight: | 222.05 g./mol | Molecular Formula: | C₁₁H₁₅BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03411946 | |
| Melting Point: | 100-106°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds, which are essential in pharmaceuticals and materials science. Additionally, the tert-butoxycarbonyl (Boc) protecting group enhances its stability and allows for selective deprotection during multi-step synthesis processes. This compound is also employed in the development of advanced organic materials, such as polymers and liquid crystals, due to its ability to introduce aromatic boronic acid functionalities into complex structures. Its versatility makes it a crucial component in medicinal chemistry for the synthesis of drug candidates and bioactive molecules.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 97.5-100 |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft3,232.23 |
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| 1.000 | 10-20 days | Ft8,403.80 |
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| 5.000 | 10-20 days | Ft39,648.72 |
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4-(tert-Butoxycarbonyl)benzeneboronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds, which are essential in pharmaceuticals and materials science. Additionally, the tert-butoxycarbonyl (Boc) protecting group enhances its stability and allows for selective deprotection during multi-step synthesis processes. This compound is also employed in the development of advanced organic materials, such as polymers and liquid crystals, due to its ability to introduce aromatic boronic acid functionalities into complex structures. Its versatility makes it a crucial component in medicinal chemistry for the synthesis of drug candidates and bioactive molecules.
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