(S)-3-((2R,5S)-5-(4-Fluorophenyl)-2-((S)-((4-fluorophenyl)amino)(4-((trimethylsilyl)oxy)phenyl)methyl)-5-((trimethylsilyl)oxy)pentanoyl)-4-phenyloxazolidin-2-one
97%
- Product Code: 44696
CAS:
272778-12-8
| Molecular Weight: | 716.96 g./mol | Molecular Formula: | C₃₉H₄₆F₂N₂O₅Si₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08460200 | |
| Melting Point: | Boiling Point: | 748.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex pharmaceutical compounds. Its structure, featuring multiple functional groups, makes it a valuable intermediate in the synthesis of biologically active molecules. The compound is often employed in the preparation of chiral drugs, where stereochemistry plays a critical role in efficacy and safety. Its fluorophenyl and oxazolidinone moieties are particularly significant in designing molecules with potential therapeutic applications, such as antimicrobial or anti-inflammatory agents. Additionally, the trimethylsilyl groups enhance its stability and reactivity, facilitating selective transformations in multi-step synthetic routes. This chemical is also explored in medicinal chemistry research for its potential in targeting specific enzymes or receptors, contributing to the development of novel treatments for various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $10.62 |
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| 0.250 | 10-20 days | $12.74 |
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| 1.000 | 10-20 days | $16.63 |
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| 5.000 | 10-20 days | $60.17 |
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(S)-3-((2R,5S)-5-(4-Fluorophenyl)-2-((S)-((4-fluorophenyl)amino)(4-((trimethylsilyl)oxy)phenyl)methyl)-5-((trimethylsilyl)oxy)pentanoyl)-4-phenyloxazolidin-2-one
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex pharmaceutical compounds. Its structure, featuring multiple functional groups, makes it a valuable intermediate in the synthesis of biologically active molecules. The compound is often employed in the preparation of chiral drugs, where stereochemistry plays a critical role in efficacy and safety. Its fluorophenyl and oxazolidinone moieties are particularly significant in designing molecules with potential therapeutic applications, such as antimicrobial or anti-inflammatory agents. Additionally, the trimethylsilyl groups enhance its stability and reactivity, facilitating selective transformations in multi-step synthetic routes. This chemical is also explored in medicinal chemistry research for its potential in targeting specific enzymes or receptors, contributing to the development of novel treatments for various diseases.
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