3-Amino-4-methylbenzeneboronic acid
98%
- Product Code: 90182
Alias:
3-Amino-4-methylphenylboronic acid
CAS:
22237-12-3
| Molecular Weight: | 150.98 g./mol | Molecular Formula: | C₇H₁₀BNO₂ |
|---|---|---|---|
| EC Number: | 000-000-0 | MDL Number: | MFCD01074640 |
| Melting Point: | 250°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a building block for the creation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form biaryl compounds, which are essential in pharmaceuticals and material science. Additionally, its amino and boronic acid functional groups make it a versatile intermediate in the development of sensors and diagnostic agents, especially for detecting sugars and other biologically relevant molecules. Its applications also extend to the field of medicinal chemistry, where it is used in the synthesis of potential drug candidates targeting various diseases.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98-100 |
| APPEARANCE | WHITE TO YELLOW TO BROWN TO GREY POWDER OR CHUNKS |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,160.00 |
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| 5.000 | 10-20 days | ฿10,080.00 |
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3-Amino-4-methylbenzeneboronic acid
This compound is primarily utilized in organic synthesis as a building block for the creation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid partner to form biaryl compounds, which are essential in pharmaceuticals and material science. Additionally, its amino and boronic acid functional groups make it a versatile intermediate in the development of sensors and diagnostic agents, especially for detecting sugars and other biologically relevant molecules. Its applications also extend to the field of medicinal chemistry, where it is used in the synthesis of potential drug candidates targeting various diseases.
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