(2-hydroxy-4-(methyl-d3)pyrimidin-5-yl)boronic acid
95%
- Product Code: 58141
CAS:
2225154-45-8
| Molecular Weight: | C5H4BD3N2O3 g./mol | Molecular Formula: | C₅H₄BD₃N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly in the development of deuterated drugs. Its boronic acid functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This is especially useful in creating complex molecules for drug discovery and material science. The deuterium substitution (methyl-d3) enhances metabolic stability, making it a key component in the design of deuterated pharmaceuticals, which often exhibit improved pharmacokinetic properties and reduced side effects. Additionally, it serves as a building block in the synthesis of pyrimidine derivatives, which are important in medicinal chemistry for their biological activity.
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-hydroxy-4-(methyl-d3)pyrimidin-5-yl)boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research, particularly in the development of deuterated drugs. Its boronic acid functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This is especially useful in creating complex molecules for drug discovery and material science. The deuterium substitution (methyl-d3) enhances metabolic stability, making it a key component in the design of deuterated pharmaceuticals, which often exhibit improved pharmacokinetic properties and reduced side effects. Additionally, it serves as a building block in the synthesis of pyrimidine derivatives, which are important in medicinal chemistry for their biological activity.
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