(S)-2-Hydroxy-3-(4-nitrophenyl)propanoic acid
97%
- Product Code: 38338
CAS:
33173-27-2
| Molecular Weight: | 211.1715 g./mol | Molecular Formula: | C₉H₉NO₅ |
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| EC Number: | MDL Number: | MFCD00039747 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
(S)-2-Hydroxy-3-(4-nitrophenyl)propanoic acid finds application primarily in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting enzyme inhibition and receptor modulation. Its structure, featuring a nitro group and a hydroxyl group, makes it a valuable building block for designing molecules with potential therapeutic properties. Additionally, it is utilized in the development of chiral catalysts and ligands for asymmetric synthesis, aiding in the creation of enantiomerically pure compounds. In medicinal chemistry, it is explored for its role in synthesizing drugs with anti-inflammatory, antimicrobial, or anticancer activities. Its versatility also extends to material science, where it contributes to the design of advanced polymers and coatings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,646.00 |
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(S)-2-Hydroxy-3-(4-nitrophenyl)propanoic acid
(S)-2-Hydroxy-3-(4-nitrophenyl)propanoic acid finds application primarily in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the production of various bioactive compounds, particularly those targeting enzyme inhibition and receptor modulation. Its structure, featuring a nitro group and a hydroxyl group, makes it a valuable building block for designing molecules with potential therapeutic properties. Additionally, it is utilized in the development of chiral catalysts and ligands for asymmetric synthesis, aiding in the creation of enantiomerically pure compounds. In medicinal chemistry, it is explored for its role in synthesizing drugs with anti-inflammatory, antimicrobial, or anticancer activities. Its versatility also extends to material science, where it contributes to the design of advanced polymers and coatings.
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