(2-(2-(methyl-d3)propan-2-yl-1,1,1,3,3,3-d6)pyridin-4-yl)boronic acid
95%
- Product Code: 56299
CAS:
2241875-88-5
| Molecular Weight: | 188.079416002 g./mol | Molecular Formula: | C₉H₅BD₉NO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of deuterated pharmaceutical compounds. Deuterated drugs, which incorporate deuterium atoms in place of hydrogen, often exhibit improved metabolic stability and pharmacokinetic properties. The boronic acid group in this molecule makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Its application is especially relevant in the development of targeted therapies and imaging agents, where precise molecular modifications are critical. Additionally, the deuterium labeling allows for the study of drug metabolism and distribution using techniques like mass spectrometry, aiding in the optimization of drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $13,541.93 |
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| 0.025 | 10-20 days | $36,162.72 |
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(2-(2-(methyl-d3)propan-2-yl-1,1,1,3,3,3-d6)pyridin-4-yl)boronic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of deuterated pharmaceutical compounds. Deuterated drugs, which incorporate deuterium atoms in place of hydrogen, often exhibit improved metabolic stability and pharmacokinetic properties. The boronic acid group in this molecule makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Its application is especially relevant in the development of targeted therapies and imaging agents, where precise molecular modifications are critical. Additionally, the deuterium labeling allows for the study of drug metabolism and distribution using techniques like mass spectrometry, aiding in the optimization of drug candidates.
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