(1R,3S,4S)-tert-Butyl 3-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate
98%
- Product Code: 70807
CAS:
1256387-87-7
| Molecular Weight: | 439.36 g./mol | Molecular Formula: | C₂₄H₃₄BN₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28386938 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
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 biologically active molecules. Its structure, featuring a boronic ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic compounds, including pharmaceuticals and agrochemicals. Additionally, the bicyclic framework and imidazole moiety in the molecule suggest potential applications in the design of drug candidates targeting various diseases, such as cancer or infectious diseases, due to their ability to interact with biological targets. Its role as a building block in drug discovery highlights its importance in creating novel therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white to light yellow Solid |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿980.00 |
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| 0.250 | 10-20 days | ฿1,510.00 |
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| 1.000 | 10-20 days | ฿4,520.00 |
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(1R,3S,4S)-tert-Butyl 3-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]imidazol-2-yl)-2-azabicyclo[2.2.1]heptane-2-carboxylate
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 biologically active molecules. Its structure, featuring a boronic ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic compounds, including pharmaceuticals and agrochemicals. Additionally, the bicyclic framework and imidazole moiety in the molecule suggest potential applications in the design of drug candidates targeting various diseases, such as cancer or infectious diseases, due to their ability to interact with biological targets. Its role as a building block in drug discovery highlights its importance in creating novel therapeutic agents.
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