(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)boronic acid
97%
- Product Code: 91038
CAS:
844501-00-4
| Molecular Weight: | 227.07 g./mol | Molecular Formula: | C₁₀H₁₈BNO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including bioactive compounds and drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group enhances its stability and facilitates selective reactions, making it a versatile building block in multi-step synthetic processes. Its applications extend to the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿675.00 |
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| 0.100 | 10-20 days | ฿1,440.00 |
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| 0.250 | 10-20 days | ฿3,222.00 |
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| 1.000 | 10-20 days | ฿9,090.00 |
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| 5.000 | 10-20 days | ฿41,400.00 |
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(1-(tert-Butoxycarbonyl)-1,2,3,6-tetrahydropyridin-4-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry, where it serves as a key intermediate in the development of pharmaceutical agents. Its boronic acid group makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in constructing complex molecules, including bioactive compounds and drug candidates. Additionally, the tert-butoxycarbonyl (Boc) protecting group enhances its stability and facilitates selective reactions, making it a versatile building block in multi-step synthetic processes. Its applications extend to the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases.
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