1-(Cbz-amino)cyclohexanecarboxylic Acid
≥97%
- Product Code: 76173
CAS:
17191-43-4
| Molecular Weight: | 277.32 g./mol | Molecular Formula: | C₁₅H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02094521 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
1-(Cbz-amino)cyclohexanecarboxylic acid is widely used in peptide synthesis as a protecting group for amino acids. The Cbz (carbobenzoxy) group shields the amino functionality during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids in the peptide chain. This compound is particularly valuable in solid-phase peptide synthesis, where selective deprotection is required to build complex peptides efficiently. Additionally, it serves as an intermediate in the production of various pharmaceuticals, including enzyme inhibitors and bioactive peptides, due to its stability and ease of removal under mild conditions. Its cyclohexane backbone also contributes to the conformational stability of the synthesized peptides, enhancing their biological activity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,680.00 |
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1-(Cbz-amino)cyclohexanecarboxylic Acid
1-(Cbz-amino)cyclohexanecarboxylic acid is widely used in peptide synthesis as a protecting group for amino acids. The Cbz (carbobenzoxy) group shields the amino functionality during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids in the peptide chain. This compound is particularly valuable in solid-phase peptide synthesis, where selective deprotection is required to build complex peptides efficiently. Additionally, it serves as an intermediate in the production of various pharmaceuticals, including enzyme inhibitors and bioactive peptides, due to its stability and ease of removal under mild conditions. Its cyclohexane backbone also contributes to the conformational stability of the synthesized peptides, enhancing their biological activity.
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