(2-(1,4-Dioxa-8-azaspiro[4.5]decan-8-ylsulfonyl)-4,5-difluorophenyl)boronic acid
98%
- Product Code: 88998
CAS:
1704074-09-8
| Molecular Weight: | 363.15 g./mol | Molecular Formula: | C₁₃H₁₆BF₂NO₆S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400355 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions, where it acts as a key intermediate. Its boronic acid functional group makes it valuable in Suzuki-Miyaura coupling, a widely employed method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The compound’s unique structure, featuring a spirocyclic dioxa-aza system, may also contribute to its stability and reactivity in these reactions. Additionally, it can be utilized in the development of bioactive compounds, where its difluorophenyl group can enhance binding affinity and metabolic stability in drug candidates. Its applications are often focused on advanced research and industrial processes in medicinal chemistry and material science.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿38,510.00 |
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(2-(1,4-Dioxa-8-azaspiro[4.5]decan-8-ylsulfonyl)-4,5-difluorophenyl)boronic acid
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions, where it acts as a key intermediate. Its boronic acid functional group makes it valuable in Suzuki-Miyaura coupling, a widely employed method for forming carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The compound’s unique structure, featuring a spirocyclic dioxa-aza system, may also contribute to its stability and reactivity in these reactions. Additionally, it can be utilized in the development of bioactive compounds, where its difluorophenyl group can enhance binding affinity and metabolic stability in drug candidates. Its applications are often focused on advanced research and industrial processes in medicinal chemistry and material science.
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