(R)-2-((((9H-FLUOREN-9-YL)METHOXY)CARBONYL)(METHYL)AMINO)-5-(TERT-BUTOXY)-5-OXOPENTANOIC ACID
98%
- Product Code: 231099
CAS:
1562442-35-6
| Molecular Weight: | 439.51 g./mol | Molecular Formula: | C₂₅H₂₉NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04974254 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in peptide synthesis as a protected chiral building block. Its main application lies in the preparation of complex peptides and peptidomimetics, where the tert-butoxy and Fmoc groups provide orthogonal protection for carboxylic acid and amine functionalities. The compound enables stepwise assembly of peptide chains with stereochemical control, making it valuable in pharmaceutical research and development, especially in synthesizing bioactive peptides with high purity and defined configuration. Commonly employed in solid-phase peptide synthesis (SPPS), it allows for mild deprotection conditions, preserving sensitive functional groups in the growing peptide chain.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $429.54 |
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| 0.250 | 10-20 days | $706.42 |
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| 1.000 | 10-20 days | $959.12 |
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(R)-2-((((9H-FLUOREN-9-YL)METHOXY)CARBONYL)(METHYL)AMINO)-5-(TERT-BUTOXY)-5-OXOPENTANOIC ACID
Used primarily in peptide synthesis as a protected chiral building block. Its main application lies in the preparation of complex peptides and peptidomimetics, where the tert-butoxy and Fmoc groups provide orthogonal protection for carboxylic acid and amine functionalities. The compound enables stepwise assembly of peptide chains with stereochemical control, making it valuable in pharmaceutical research and development, especially in synthesizing bioactive peptides with high purity and defined configuration. Commonly employed in solid-phase peptide synthesis (SPPS), it allows for mild deprotection conditions, preserving sensitive functional groups in the growing peptide chain.
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