(3aR,4R,6S,6aS) -4-(tert-butoxycarbonylaMino) -3-(pentan-3-yl)-4,5,6,6a-tetrahydro -3aH-cyclopenta[d]isoxazole -6-carboxylic acid
99%
- Product Code: 36719
CAS:
316173-28-1
| Molecular Weight: | 413.55 g./mol | Molecular Formula: | C₂₁H₃₉N₃O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18252295 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the development of pharmaceuticals. Its unique structure makes it a valuable intermediate in the production of biologically active molecules, such as enzyme inhibitors or receptor modulators. It is often employed in medicinal chemistry research to create novel drug candidates targeting specific diseases. Additionally, its stereochemistry allows for precise control in asymmetric synthesis, making it useful in the preparation of chiral compounds. The tert-butoxycarbonyl (Boc) protecting group in its structure facilitates selective reactions, enabling efficient multi-step synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Powder |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $25.75 |
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| 1.000 | 10-20 days | $111.30 |
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| 5.000 | 10-20 days | $274.92 |
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| 25.000 | 10-20 days | $830.16 |
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(3aR,4R,6S,6aS) -4-(tert-butoxycarbonylaMino) -3-(pentan-3-yl)-4,5,6,6a-tetrahydro -3aH-cyclopenta[d]isoxazole -6-carboxylic acid
This chemical is primarily utilized in the synthesis of complex organic compounds, particularly in the development of pharmaceuticals. Its unique structure makes it a valuable intermediate in the production of biologically active molecules, such as enzyme inhibitors or receptor modulators. It is often employed in medicinal chemistry research to create novel drug candidates targeting specific diseases. Additionally, its stereochemistry allows for precise control in asymmetric synthesis, making it useful in the preparation of chiral compounds. The tert-butoxycarbonyl (Boc) protecting group in its structure facilitates selective reactions, enabling efficient multi-step synthetic processes.
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