(1R,2S)-2-Amino-1-(Boc-amino)cyclopentane
≥95%
- Product Code: 69057
CAS:
721395-15-9
| Molecular Weight: | 200.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12828694 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in the synthesis of peptides and peptidomimetics, where it serves as a building block for creating complex molecular structures. Its Boc (tert-butoxycarbonyl) protecting group ensures stability during chemical reactions, allowing selective deprotection when needed. It is also employed in the development of pharmaceuticals, particularly in the design of enzyme inhibitors and receptor ligands, due to its chiral cyclopentane backbone, which can mimic natural amino acid conformations. Additionally, it finds application in organic synthesis for constructing cyclic compounds with specific stereochemistry, aiding in the study of structure-activity relationships in drug discovery.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 95-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,481.00 |
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| 1.000 | 10-20 days | ฿12,618.00 |
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| 5.000 | 10-20 days | ฿46,449.00 |
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(1R,2S)-2-Amino-1-(Boc-amino)cyclopentane
This chemical is primarily used in the synthesis of peptides and peptidomimetics, where it serves as a building block for creating complex molecular structures. Its Boc (tert-butoxycarbonyl) protecting group ensures stability during chemical reactions, allowing selective deprotection when needed. It is also employed in the development of pharmaceuticals, particularly in the design of enzyme inhibitors and receptor ligands, due to its chiral cyclopentane backbone, which can mimic natural amino acid conformations. Additionally, it finds application in organic synthesis for constructing cyclic compounds with specific stereochemistry, aiding in the study of structure-activity relationships in drug discovery.
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