cis-2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid
98%
- Product Code: 54740
CAS:
136315-70-3
| Molecular Weight: | 229.2729 g./mol | Molecular Formula: | C₁₁H₁₉NO₄ |
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| EC Number: | MDL Number: | MFCD00800539 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the synthesis of peptides and other organic compounds, serving as a protected amino acid derivative. Its structure, featuring a tert-butoxycarbonyl (Boc) group, makes it valuable in peptide chemistry for protecting the amino group during reactions. It is often employed in solid-phase peptide synthesis (SPPS) to build complex peptide chains, ensuring selective deprotection and coupling steps. Additionally, it finds application in the preparation of cyclopentane-based drug candidates, where the cyclopentane ring contributes to the conformational rigidity of the molecule, enhancing its binding affinity to biological targets. Its stability and compatibility with various reaction conditions make it a versatile intermediate in medicinal chemistry and pharmaceutical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,386.00 |
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cis-2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid
This chemical is primarily used in the synthesis of peptides and other organic compounds, serving as a protected amino acid derivative. Its structure, featuring a tert-butoxycarbonyl (Boc) group, makes it valuable in peptide chemistry for protecting the amino group during reactions. It is often employed in solid-phase peptide synthesis (SPPS) to build complex peptide chains, ensuring selective deprotection and coupling steps. Additionally, it finds application in the preparation of cyclopentane-based drug candidates, where the cyclopentane ring contributes to the conformational rigidity of the molecule, enhancing its binding affinity to biological targets. Its stability and compatibility with various reaction conditions make it a versatile intermediate in medicinal chemistry and pharmaceutical research.
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