(S)-4-Methyl-2-(methyl((2-(trimethylsilyl)ethoxy)carbonyl)amino)pentanoic acid
98%
- Product Code: 38532
CAS:
2411590-92-4
| Molecular Weight: | 289.4433 g./mol | Molecular Formula: | C₁₃H₂₇NO₄Si |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in peptide synthesis as a protecting group for amino acids. Its structure includes a trimethylsilyl group, which enhances stability and facilitates selective deprotection under mild conditions. This makes it particularly useful in solid-phase peptide synthesis, where controlled removal of protecting groups is essential for constructing complex peptide chains. Additionally, its chiral nature allows for the synthesis of enantiomerically pure peptides, which is critical in pharmaceutical applications where stereochemistry influences biological activity. The compound’s design ensures compatibility with various coupling reagents and solvents, making it a versatile tool in organic and medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,133.00 |
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(S)-4-Methyl-2-(methyl((2-(trimethylsilyl)ethoxy)carbonyl)amino)pentanoic acid
This compound is primarily utilized in peptide synthesis as a protecting group for amino acids. Its structure includes a trimethylsilyl group, which enhances stability and facilitates selective deprotection under mild conditions. This makes it particularly useful in solid-phase peptide synthesis, where controlled removal of protecting groups is essential for constructing complex peptide chains. Additionally, its chiral nature allows for the synthesis of enantiomerically pure peptides, which is critical in pharmaceutical applications where stereochemistry influences biological activity. The compound’s design ensures compatibility with various coupling reagents and solvents, making it a versatile tool in organic and medicinal chemistry research.
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