3,3,3-Trifluoro-2-hydroxy-2-phenylpropanoic acid
95%
- Product Code: 64293
CAS:
55519-22-7
| Molecular Weight: | 220.15 g./mol | Molecular Formula: | C₉H₇F₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06208429 | |
| Melting Point: | Boiling Point: | 333.8±42.0 °C(Predicted) | |
| Density: | 1.486±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its unique structure, featuring both trifluoromethyl and hydroxyl groups, makes it valuable for developing drugs with enhanced metabolic stability and bioavailability. It is particularly significant in the production of anti-inflammatory and analgesic medications, where its incorporation can improve the efficacy and safety profiles of the final drug products. Additionally, it finds applications in organic synthesis as a building block for creating complex molecules with potential therapeutic properties. Its role in facilitating the introduction of fluorine atoms into organic compounds is also noteworthy, as fluorinated compounds often exhibit desirable biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $502.66 |
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| 0.250 | 10-20 days | $854.80 |
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| 1.000 | 10-20 days | $2,307.63 |
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3,3,3-Trifluoro-2-hydroxy-2-phenylpropanoic acid
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its unique structure, featuring both trifluoromethyl and hydroxyl groups, makes it valuable for developing drugs with enhanced metabolic stability and bioavailability. It is particularly significant in the production of anti-inflammatory and analgesic medications, where its incorporation can improve the efficacy and safety profiles of the final drug products. Additionally, it finds applications in organic synthesis as a building block for creating complex molecules with potential therapeutic properties. Its role in facilitating the introduction of fluorine atoms into organic compounds is also noteworthy, as fluorinated compounds often exhibit desirable biological activities.
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