trans-2-Amino-1-cyclohexanecarboxylic acid
98%
- Product Code: 54430
CAS:
5691-19-0
| Molecular Weight: | 143.18 g./mol | Molecular Formula: | C₇H₁₃NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00145418 | |
| Melting Point: | ~255℃ (dec.) | Boiling Point: | 261.28°C (rough estimate) |
| Density: | 1.1095 (rough estimate) | Storage Condition: | room temperature |
Product Description:
Trans-2-Amino-1-cyclohexanecarboxylic acid is primarily used in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the production of various pharmaceutical compounds. Its structure makes it valuable for the synthesis of peptidomimetics, which are molecules that mimic peptides and are used in drug development to enhance stability and bioavailability. Additionally, it is utilized in the study of enzyme inhibitors, particularly those targeting proteases, due to its cyclohexane backbone and amino acid functionality. This compound also finds applications in the development of chiral catalysts and ligands, aiding in asymmetric synthesis processes. Its unique properties make it a versatile building block in the creation of complex molecules for therapeutic and research purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $1,216.47 |
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trans-2-Amino-1-cyclohexanecarboxylic acid
Trans-2-Amino-1-cyclohexanecarboxylic acid is primarily used in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the production of various pharmaceutical compounds. Its structure makes it valuable for the synthesis of peptidomimetics, which are molecules that mimic peptides and are used in drug development to enhance stability and bioavailability. Additionally, it is utilized in the study of enzyme inhibitors, particularly those targeting proteases, due to its cyclohexane backbone and amino acid functionality. This compound also finds applications in the development of chiral catalysts and ligands, aiding in asymmetric synthesis processes. Its unique properties make it a versatile building block in the creation of complex molecules for therapeutic and research purposes.
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