2-Carboxybenzeneboronic acid
97%
- Product Code: 89873
Alias:
2-carboxyphenylboronic acid ,2-carboxyphenylboronic acid, 2-carboxyphenylboronic acid
CAS:
149105-19-1
| Molecular Weight: | 201.97 g./mol | Molecular Formula: | C₇H₇BO₄₂H₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318118 | |
| Melting Point: | 138-141°C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Used in organic synthesis as a building block for creating complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and materials science. It serves as a key intermediate in the production of bioactive compounds, including drugs and agrochemicals. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose detection and other biochemical applications. Its boronic acid group also enables its use in polymer chemistry for creating functional materials with specific properties.
Product Specification:
| Test | Specification |
|---|---|
| PURITYNEUTRALIZATION TITRATION | 97-112 |
| WATER MOLE EQ | 1.7-2.3 |
| APPEARANCE | WHITE TO BEIGE POWDER |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿300.00 |
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| 1.000 | 10-20 days | ฿560.00 |
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| 5.000 | 10-20 days | ฿2,210.00 |
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| 25.000 | 10-20 days | ฿8,410.00 |
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2-Carboxybenzeneboronic acid
Used in organic synthesis as a building block for creating complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and materials science. It serves as a key intermediate in the production of bioactive compounds, including drugs and agrochemicals. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with diols and sugars, making it useful in glucose detection and other biochemical applications. Its boronic acid group also enables its use in polymer chemistry for creating functional materials with specific properties.
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