Phenylboronic Acid-d5
98%
- Product Code: 64574
CAS:
215527-70-1
| Molecular Weight: | 126.9604 g./mol | Molecular Formula: | C₆H₂D₅BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02093711 | |
| Melting Point: | 217-220°C (lit.) | Boiling Point: | 265.9°C at 760 mmHg |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Phenylboronic Acid-d5 is primarily used in research and development, particularly in the field of organic synthesis and medicinal chemistry. It serves as a deuterated analog of phenylboronic acid, enabling scientists to study reaction mechanisms and metabolic pathways with greater precision using techniques like NMR spectroscopy. Its deuterium labeling allows for tracking and analysis in complex chemical and biological systems without interference from non-deuterated counterparts. Additionally, it is employed in the development of boron-based drugs and as a building block in Suzuki-Miyaura cross-coupling reactions, which are pivotal in creating pharmaceuticals and advanced materials. Its application extends to the study of carbohydrate interactions and sensors, where boronic acids play a key role in molecular recognition.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $14.09 |
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| 0.250 | 10-20 days | $22.54 |
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| 1.000 | 10-20 days | $84.07 |
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Phenylboronic Acid-d5
Phenylboronic Acid-d5 is primarily used in research and development, particularly in the field of organic synthesis and medicinal chemistry. It serves as a deuterated analog of phenylboronic acid, enabling scientists to study reaction mechanisms and metabolic pathways with greater precision using techniques like NMR spectroscopy. Its deuterium labeling allows for tracking and analysis in complex chemical and biological systems without interference from non-deuterated counterparts. Additionally, it is employed in the development of boron-based drugs and as a building block in Suzuki-Miyaura cross-coupling reactions, which are pivotal in creating pharmaceuticals and advanced materials. Its application extends to the study of carbohydrate interactions and sensors, where boronic acids play a key role in molecular recognition.
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