3-(N-METHYLAMINOCARBONYL)PHENYLBORONIC ACID
98%
- Product Code: 90008
Alias:
3-Methylcarbamoylphenylboronic acid 3-(methylcarbamoyl)phenylboronic acid 3-(N-methylaminoacyl)phenylboronic acid (3-(methylcarbamoyl)phenyl)boronic acid
CAS:
832695-88-2
| Molecular Weight: | 178.98 g./mol | Molecular Formula: | C₈H₁₀BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 114-124°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex molecules. Additionally, it is employed in the development of boron-containing drugs, which are explored for their potential in treating diseases like cancer and inflammation. Its boronic acid group also makes it useful in sensor technologies for detecting sugars and other biologically relevant molecules.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98 100% |
| MP | 114 124? |
| APPEARANCE | White crystalline powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,601.00 |
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| 5.000 | 10-20 days | ฿7,578.00 |
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3-(N-METHYLAMINOCARBONYL)PHENYLBORONIC ACID
Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds to create complex molecules. Additionally, it is employed in the development of boron-containing drugs, which are explored for their potential in treating diseases like cancer and inflammation. Its boronic acid group also makes it useful in sensor technologies for detecting sugars and other biologically relevant molecules.
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