cis-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexanecarboxylic acid
97%
- Product Code: 196744
CAS:
147900-45-6
| Molecular Weight: | 365.42 g./mol | Molecular Formula: | C₂₂H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01862344 | |
| Melting Point: | Boiling Point: | 596.9 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, enabling selective coupling reactions. Its structure supports solid-phase peptide synthesis (SPPS), particularly in Fmoc strategy, where the Fmoc group provides temporary N-terminal protection. The cyclohexane backbone introduces conformational constraints, useful in designing peptides with specific secondary structures. It also finds use in synthesizing peptidomimetics and bioactive molecules requiring stereochemical control. The carboxylic acid functionality allows attachment to resin supports or further amide bond formation. Its stability under mild conditions makes it suitable for multi-step syntheses in pharmaceutical and biochemical research.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,010.00 |
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| 250mg | 10-20 days | ฿3,480.00 |
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| 1g | 10-20 days | ฿5,720.00 |
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| 5g | 10-20 days | ฿24,700.00 |
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cis-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)cyclohexanecarboxylic acid
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, enabling selective coupling reactions. Its structure supports solid-phase peptide synthesis (SPPS), particularly in Fmoc strategy, where the Fmoc group provides temporary N-terminal protection. The cyclohexane backbone introduces conformational constraints, useful in designing peptides with specific secondary structures. It also finds use in synthesizing peptidomimetics and bioactive molecules requiring stereochemical control. The carboxylic acid functionality allows attachment to resin supports or further amide bond formation. Its stability under mild conditions makes it suitable for multi-step syntheses in pharmaceutical and biochemical research.
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