(R)-3-((tert-Butoxycarbonyl)amino)-4-(m-tolyl)butanoic acid
98%
- Product Code: 104260
CAS:
269398-83-6
| Molecular Weight: | 293.36 g./mol | Molecular Formula: | C₁₆H₂₃NO₄ |
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| EC Number: | MDL Number: | MFCD01860925 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as a key intermediate in the production of various biologically active molecules, particularly in the development of peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable for controlled reactions in peptide coupling processes. Additionally, it is employed in the synthesis of inhibitors and modulators targeting specific enzymes or receptors, contributing to research in drug discovery and therapeutic development. Its application extends to the preparation of chiral compounds, where its stereochemistry plays a critical role in achieving desired pharmacological properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,581.00 |
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| 0.250 | 10-20 days | ฿6,840.00 |
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| 1.000 | 10-20 days | ฿17,010.00 |
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(R)-3-((tert-Butoxycarbonyl)amino)-4-(m-tolyl)butanoic acid
This compound is primarily utilized in the pharmaceutical and organic synthesis industries. It serves as a key intermediate in the production of various biologically active molecules, particularly in the development of peptide-based drugs. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable for controlled reactions in peptide coupling processes. Additionally, it is employed in the synthesis of inhibitors and modulators targeting specific enzymes or receptors, contributing to research in drug discovery and therapeutic development. Its application extends to the preparation of chiral compounds, where its stereochemistry plays a critical role in achieving desired pharmacological properties.
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