(S)-3-Amino-3-(3-nitrophenyl)propanoic acid
97%
- Product Code: 38437
CAS:
734529-57-8
| Molecular Weight: | 210.19 g./mol | Molecular Formula: | C₉H₁₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04113693 | |
| Melting Point: | Boiling Point: | 384.5°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
(S)-3-Amino-3-(3-nitrophenyl)propanoic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring both an amino group and a nitro-substituted phenyl ring, makes it a valuable building block for designing molecules with potential therapeutic effects. Researchers often employ it in the development of enzyme inhibitors, receptor modulators, and other drug candidates. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug design, enhancing the efficacy and selectivity of potential medications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,034.00 |
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| 1.000 | 10-20 days | ฿5,112.00 |
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| 5.000 | 10-20 days | ฿16,713.00 |
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| 10.000 | 10-20 days | ฿33,318.00 |
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(S)-3-Amino-3-(3-nitrophenyl)propanoic acid
(S)-3-Amino-3-(3-nitrophenyl)propanoic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring both an amino group and a nitro-substituted phenyl ring, makes it a valuable building block for designing molecules with potential therapeutic effects. Researchers often employ it in the development of enzyme inhibitors, receptor modulators, and other drug candidates. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug design, enhancing the efficacy and selectivity of potential medications.
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