2-(Hydroxymethyl)phenylboronic acid cyclic monoester
98%
- Product Code: 83302
CAS:
5735-41-1
Properties:
3
| Molecular Weight: | 133.94 g./mol | Molecular Formula: | C₇H₇BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | 5735-41-1 | |
| Melting Point: | 98-100°C | Boiling Point: | 237.2ºC |
| Density: | 1.18g/cm3 | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of enzyme inhibitors and antiviral agents. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic molecules in drug development. Additionally, it is employed in the preparation of boron-containing compounds for cancer therapy and diagnostic imaging. Its boronic acid functionality makes it valuable in glucose sensing applications, particularly in the development of continuous glucose monitoring systems for diabetes management. Also utilized in material science for modifying surfaces and creating functional polymers with specific binding properties.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to Yellow to Brown Solid, Powder, Crystals, Crystalline Powder and/or Chunks |
| Proton NMR Spectrum | Conforms to Structure |
| Purity | 97.5 100% |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿570.00 |
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| 5.000 | 10-20 days | ฿2,280.00 |
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| 25.000 | 10-20 days | ฿7,900.00 |
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| 100.000 | 10-20 days | ฿30,200.00 |
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2-(Hydroxymethyl)phenylboronic acid cyclic monoester
Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of enzyme inhibitors and antiviral agents. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic molecules in drug development. Additionally, it is employed in the preparation of boron-containing compounds for cancer therapy and diagnostic imaging. Its boronic acid functionality makes it valuable in glucose sensing applications, particularly in the development of continuous glucose monitoring systems for diabetes management. Also utilized in material science for modifying surfaces and creating functional polymers with specific binding properties.
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