(R)-3-Amino-3-(2-nitrophenyl)propanoic acid
98%
- Product Code: 87157
CAS:
756814-14-9
| Molecular Weight: | 210.19 g./mol | Molecular Formula: | C₉H₁₀N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04113648 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dark, dry, sealed |
Product Description:
(R)-3-Amino-3-(2-nitrophenyl)propanoic acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of chiral compounds, which are essential for creating enantiomerically pure drugs. This compound is particularly valuable in the synthesis of beta-amino acids, which are crucial building blocks for peptides and peptidomimetics. These peptides often exhibit enhanced stability and bioavailability, making them important in drug design. Additionally, the nitro group present in the molecule allows for further functionalization, enabling the creation of diverse derivatives for biological activity screening. Its application is also seen in asymmetric synthesis, where it aids in the production of optically active molecules with potential therapeutic properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,445.00 |
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| 0.100 | 10-20 days | ฿3,627.00 |
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| 1.000 | 10-20 days | ฿13,608.00 |
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(R)-3-Amino-3-(2-nitrophenyl)propanoic acid
(R)-3-Amino-3-(2-nitrophenyl)propanoic acid is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of chiral compounds, which are essential for creating enantiomerically pure drugs. This compound is particularly valuable in the synthesis of beta-amino acids, which are crucial building blocks for peptides and peptidomimetics. These peptides often exhibit enhanced stability and bioavailability, making them important in drug design. Additionally, the nitro group present in the molecule allows for further functionalization, enabling the creation of diverse derivatives for biological activity screening. Its application is also seen in asymmetric synthesis, where it aids in the production of optically active molecules with potential therapeutic properties.
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