(S)-3-Amino-4-(4-nitrophenyl)butanoic acid hydrochloride
95%
- Product Code: 81929
CAS:
331763-77-0
| Molecular Weight: | 260.674 g./mol | Molecular Formula: | C₁₀H₁₃ClN₂O₄ |
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| EC Number: | MDL Number: | MFCD01861017 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas protection |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring both an amino group and a nitro-substituted phenyl ring, makes it a valuable intermediate in the creation of bioactive compounds. It is often employed in the preparation of enzyme inhibitors and receptor ligands, where its stereochemistry plays a critical role in achieving specificity and efficacy. Additionally, it serves as a building block in the design of potential therapeutic agents targeting neurological and cardiovascular disorders. Its hydrochloride form enhances solubility, facilitating its use in various experimental and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £157.14 |
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| 0.250 | 10-20 days | £261.77 |
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(S)-3-Amino-4-(4-nitrophenyl)butanoic acid hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring both an amino group and a nitro-substituted phenyl ring, makes it a valuable intermediate in the creation of bioactive compounds. It is often employed in the preparation of enzyme inhibitors and receptor ligands, where its stereochemistry plays a critical role in achieving specificity and efficacy. Additionally, it serves as a building block in the design of potential therapeutic agents targeting neurological and cardiovascular disorders. Its hydrochloride form enhances solubility, facilitating its use in various experimental and industrial processes.
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