(3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(trifluoromethylsulfonyloxy)-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate
98%
- Product Code: 92875
CAS:
115375-60-5
| Molecular Weight: | 462.52 g./mol | Molecular Formula: | C₂₂H₂₉F₃O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18252939 | |
| Melting Point: | Boiling Point: | 491.9±45.0 °C(Predicted) | |
| Density: | 1.32±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex steroid derivatives. It serves as a key intermediate in the preparation of biologically active compounds, including pharmaceuticals targeting hormonal disorders and anti-inflammatory agents. Its trifluoromethylsulfonyloxy group makes it a valuable precursor for nucleophilic substitution reactions, enabling the introduction of various functional groups into the steroid backbone. Additionally, it is employed in research settings to study the structure-activity relationships of steroid-based molecules, aiding in the design of more effective therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $887.62 |
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| 0.250 | 10-20 days | $1,479.37 |
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(3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-(trifluoromethylsulfonyloxy)-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of complex steroid derivatives. It serves as a key intermediate in the preparation of biologically active compounds, including pharmaceuticals targeting hormonal disorders and anti-inflammatory agents. Its trifluoromethylsulfonyloxy group makes it a valuable precursor for nucleophilic substitution reactions, enabling the introduction of various functional groups into the steroid backbone. Additionally, it is employed in research settings to study the structure-activity relationships of steroid-based molecules, aiding in the design of more effective therapeutic agents.
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