2-Amino-3-methyl-3-sulfino-4-(1H-1,2,3-triazol-1-yl)butanoic acid
98%
- Product Code: 78596
CAS:
118175-11-4
| Molecular Weight: | 248.26 g./mol | Molecular Formula: | C₇H₁₂N₄O₄S |
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| EC Number: | MDL Number: | MFCD13191753 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in biochemical research and pharmaceutical development due to its unique structure, which combines amino, sulfino, and triazole functional groups. It serves as a precursor or intermediate in the synthesis of more complex molecules, particularly those targeting enzyme inhibition or receptor modulation. Its triazole moiety makes it valuable in designing compounds with potential antimicrobial or antiviral properties. Additionally, it is explored in peptide chemistry for creating modified amino acids that can enhance the stability or activity of therapeutic peptides. Its sulfino group also contributes to its role in studies involving redox reactions and sulfur metabolism.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $2,232.62 |
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| 0.250 | 10-20 days | $3,348.57 |
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2-Amino-3-methyl-3-sulfino-4-(1H-1,2,3-triazol-1-yl)butanoic acid
This chemical is primarily utilized in biochemical research and pharmaceutical development due to its unique structure, which combines amino, sulfino, and triazole functional groups. It serves as a precursor or intermediate in the synthesis of more complex molecules, particularly those targeting enzyme inhibition or receptor modulation. Its triazole moiety makes it valuable in designing compounds with potential antimicrobial or antiviral properties. Additionally, it is explored in peptide chemistry for creating modified amino acids that can enhance the stability or activity of therapeutic peptides. Its sulfino group also contributes to its role in studies involving redox reactions and sulfur metabolism.
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