2-(sec-Butyl-d9)-6-chloropyridine-4-boronic acid
95%
- Product Code: 62740
CAS:
2225151-89-1
| Molecular Weight: | 222.524476002 g./mol | Molecular Formula: | C₉H₄BClD₉NO₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various active pharmaceutical ingredients (APIs). Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the deuterated sec-butyl group enhances its utility in studies involving isotopic labeling, aiding in metabolic and pharmacokinetic research. This chemical is particularly relevant in the creation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. Its stability and reactivity make it a versatile tool in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿269,620.00 |
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-
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| 0.025 | 10-20 days | ฿720,000.00 |
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2-(sec-Butyl-d9)-6-chloropyridine-4-boronic acid
This compound is primarily used in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various active pharmaceutical ingredients (APIs). Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the deuterated sec-butyl group enhances its utility in studies involving isotopic labeling, aiding in metabolic and pharmacokinetic research. This chemical is particularly relevant in the creation of compounds with potential therapeutic applications, such as antiviral or anticancer agents. Its stability and reactivity make it a versatile tool in medicinal chemistry and drug discovery processes.
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