8-Nonenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-
97%
- Product Code: 36510
CAS:
300831-21-4
| Molecular Weight: | 271.35 g./mol | Molecular Formula: | C₁₄H₂₅NO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 422.7±45.0℃(Predicted) | |
| Density: | 1.035±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily utilized in the synthesis of peptides and other bioactive molecules due to its role as a protected amino acid derivative. Its structure, featuring a Boc (tert-butoxycarbonyl) protecting group, makes it valuable in organic synthesis, particularly in peptide coupling reactions where selective protection and deprotection strategies are required. It is often employed in the development of pharmaceuticals, especially in the production of peptide-based drugs, where it helps maintain the integrity of the amino acid during complex synthetic processes. Additionally, it can be used in research to study enzyme interactions and biochemical pathways involving amino acids.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $199.01 |
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| 5.000 | 10-20 days | $597.30 |
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| 10.000 | 10-20 days | $995.32 |
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8-Nonenoic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, (2S)-
This compound is primarily utilized in the synthesis of peptides and other bioactive molecules due to its role as a protected amino acid derivative. Its structure, featuring a Boc (tert-butoxycarbonyl) protecting group, makes it valuable in organic synthesis, particularly in peptide coupling reactions where selective protection and deprotection strategies are required. It is often employed in the development of pharmaceuticals, especially in the production of peptide-based drugs, where it helps maintain the integrity of the amino acid during complex synthetic processes. Additionally, it can be used in research to study enzyme interactions and biochemical pathways involving amino acids.
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