(2-chloro-6-(propan-2-yl-d7)pyridin-4-yl)boronic acid
95%
- Product Code: 58116
CAS:
2241875-95-4
| Molecular Weight: | 206.485572446 g./mol | Molecular Formula: | C₈H₄BClD₇NO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This chemical is primarily used in the field of pharmaceutical research and development, particularly in the synthesis of deuterated compounds. Deuterated molecules, where hydrogen atoms are replaced with deuterium, are valuable in drug discovery as they can improve the metabolic stability and pharmacokinetic properties of potential drug candidates. The boronic acid group in this compound makes it a versatile intermediate in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This enables the creation of complex organic molecules, including those with potential therapeutic applications. Additionally, its deuterated isopropyl group can be utilized in mechanistic studies and isotopic labeling to track the behavior of molecules in biological systems. Its application is thus significant in advancing medicinal chemistry and understanding drug interactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿269,620.00 |
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| 0.025 | 10-20 days | ฿720,000.00 |
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(2-chloro-6-(propan-2-yl-d7)pyridin-4-yl)boronic acid
This chemical is primarily used in the field of pharmaceutical research and development, particularly in the synthesis of deuterated compounds. Deuterated molecules, where hydrogen atoms are replaced with deuterium, are valuable in drug discovery as they can improve the metabolic stability and pharmacokinetic properties of potential drug candidates. The boronic acid group in this compound makes it a versatile intermediate in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This enables the creation of complex organic molecules, including those with potential therapeutic applications. Additionally, its deuterated isopropyl group can be utilized in mechanistic studies and isotopic labeling to track the behavior of molecules in biological systems. Its application is thus significant in advancing medicinal chemistry and understanding drug interactions.
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