(1S,4R)-(-)-4-(Boc-amino)-2-cyclopentene-1-carboxylic acid
98%
- Product Code: 104120
CAS:
151907-79-8
| Molecular Weight: | 227.26 g./mol | Molecular Formula: | C₁₁H₁₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00211287 | |
| Melting Point: | 152.9 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various bioactive compounds, including antiviral and anticancer agents. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. Its chiral structure is advantageous in the creation of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. Additionally, it is employed in peptide chemistry for the construction of cyclic peptides, which are important in drug design due to their stability and specificity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,230.00 |
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| 0.250 | 10-20 days | ฿1,980.00 |
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(1S,4R)-(-)-4-(Boc-amino)-2-cyclopentene-1-carboxylic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research and development. It serves as a key intermediate in the production of various bioactive compounds, including antiviral and anticancer agents. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling controlled reactions in multi-step synthetic processes. Its chiral structure is advantageous in the creation of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. Additionally, it is employed in peptide chemistry for the construction of cyclic peptides, which are important in drug design due to their stability and specificity.
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