tert-Butyl 4-(3-amino-6-((1S,3S,4S)-4-((tert-butyldimethylsilyl)oxy)-3-fluorocyclohexyl)pyrazin-2-yl)-2-fluorobenzoate
97%
- Product Code: 113206
CAS:
1715032-87-3
| Molecular Weight: | 519.70 g./mol | Molecular Formula: | C₂₇H₃₉F₂N₃O₃Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30609554 | |
| Melting Point: | Boiling Point: | 571.3±50.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its structure, featuring multiple functional groups such as amino, fluoro, and silyl-protected hydroxyl, makes it a valuable building block for the development of targeted therapies. It is often employed in the preparation of compounds designed for oncology and other therapeutic areas where precise molecular interactions are crucial. The presence of fluorine atoms enhances the metabolic stability and bioavailability of the resulting drugs, while the silyl protection allows for controlled deprotection during synthesis. Researchers leverage its versatility to create molecules with improved efficacy and reduced side effects, particularly in the design of kinase inhibitors and other small-molecule drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿954.00 |
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| 0.250 | 10-20 days | ฿1,935.00 |
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tert-Butyl 4-(3-amino-6-((1S,3S,4S)-4-((tert-butyldimethylsilyl)oxy)-3-fluorocyclohexyl)pyrazin-2-yl)-2-fluorobenzoate
This chemical is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex drug molecules. Its structure, featuring multiple functional groups such as amino, fluoro, and silyl-protected hydroxyl, makes it a valuable building block for the development of targeted therapies. It is often employed in the preparation of compounds designed for oncology and other therapeutic areas where precise molecular interactions are crucial. The presence of fluorine atoms enhances the metabolic stability and bioavailability of the resulting drugs, while the silyl protection allows for controlled deprotection during synthesis. Researchers leverage its versatility to create molecules with improved efficacy and reduced side effects, particularly in the design of kinase inhibitors and other small-molecule drugs.
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