(S)-N-[4-(2,5-Dioxooxazolidin-4-yl)butyl]-2,2,2-trifluoroacetamide
≥98%
- Product Code: 96568
CAS:
42267-27-6
Molecular Weight: | 268.19 g./mol | Molecular Formula: | C₉H₁₁F₃N₂O₄ |
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EC Number: | MDL Number: | MFCD11046652 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
Used in the synthesis of chiral compounds, particularly in pharmaceutical research where enantiomeric purity is crucial. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) with specific stereochemical configurations. Its application extends to the preparation of biologically active molecules, including potential drugs targeting neurological and metabolic disorders. The compound is also utilized in organic synthesis for constructing complex molecular architectures, often in the context of peptidomimetics and other bioactive molecules. Its trifluoroacetamide group enhances stability and reactivity, making it valuable in multi-step synthetic processes.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White - Almost white Crystal - Powder |
PURITY | 97.5-100 |
Specific rotation a20DC3 Dioxane | -34.0--30.0 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿390.00 |
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1.000 | 10-20 days | ฿1,230.00 |
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5.000 | 10-20 days | ฿5,400.00 |
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25.000 | 10-20 days | ฿12,960.00 |
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100.000 | 10-20 days | ฿38,880.00 |
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(S)-N-[4-(2,5-Dioxooxazolidin-4-yl)butyl]-2,2,2-trifluoroacetamide
Used in the synthesis of chiral compounds, particularly in pharmaceutical research where enantiomeric purity is crucial. It serves as a key intermediate in the development of active pharmaceutical ingredients (APIs) with specific stereochemical configurations. Its application extends to the preparation of biologically active molecules, including potential drugs targeting neurological and metabolic disorders. The compound is also utilized in organic synthesis for constructing complex molecular architectures, often in the context of peptidomimetics and other bioactive molecules. Its trifluoroacetamide group enhances stability and reactivity, making it valuable in multi-step synthetic processes.
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