(3-Fluoro-4-(thiomorpholinomethyl)phenyl)boronic acid
95%
- Product Code: 36656
CAS:
1334171-29-7
| Molecular Weight: | 269.1002232 g./mol | Molecular Formula: | C₁₁H₁₃BFNO₃S |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for the formation of carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the thiomorpholine moiety enhances its solubility and stability in various reaction conditions, facilitating its use in diverse synthetic pathways. Additionally, it may find applications in the development of bioactive compounds due to its unique structural features, which can influence molecular interactions and binding properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft109,766.61 |
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| 0.250 | 10-20 days | Ft183,073.64 |
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| 1.000 | 10-20 days | Ft512,761.35 |
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(3-Fluoro-4-(thiomorpholinomethyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for the formation of carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the thiomorpholine moiety enhances its solubility and stability in various reaction conditions, facilitating its use in diverse synthetic pathways. Additionally, it may find applications in the development of bioactive compounds due to its unique structural features, which can influence molecular interactions and binding properties.
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