(S)-2-Hydroxy-3-(4-nitrophenyl)propanoic acid

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Reagent Code: #38338
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CAS Number 33173-27-2

science Other reagents with same CAS 33173-27-2

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Weight 211.1715 g/mol
Formula C₉H₉NO₅
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MDL Number MFCD00039747
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(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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inventory 100mg
10-20 days ฿11,646.00

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(S)-2-Hydroxy-3-(4-nitrophenyl)propanoic acid
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(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 c

(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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