(S)-2-((tert-Butoxycarbonyl)amino)-2-(m-tolyl)acetic acid
≥95%
- Product Code: 38084
CAS:
1217677-36-5
| Molecular Weight: | 265.31 g./mol | Molecular Formula: | C₁₄H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01632531 | |
| Melting Point: | Boiling Point: | 420.4±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the production of chiral molecules, particularly in the development of drugs targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex organic syntheses, making it valuable in medicinal chemistry. Additionally, it is utilized in research to study enzyme interactions and receptor binding due to its chiral structure, which mimics natural amino acids. Its applications extend to the development of therapeutic agents for conditions like inflammation, cancer, and metabolic disorders.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,905.00 |
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| 1.000 | 10-20 days | ฿9,819.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-2-(m-tolyl)acetic acid
This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the production of chiral molecules, particularly in the development of drugs targeting specific biological pathways. Its tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during complex organic syntheses, making it valuable in medicinal chemistry. Additionally, it is utilized in research to study enzyme interactions and receptor binding due to its chiral structure, which mimics natural amino acids. Its applications extend to the development of therapeutic agents for conditions like inflammation, cancer, and metabolic disorders.
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