(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((R)-1-(tert-butoxycarbonyl)piperidin-3-yl)propanoic acid
95%
- Product Code: 232426
CAS:
1251904-14-9
Molecular Weight: | 494.59 g./mol | Molecular Formula: | C₂₈H₃₄N₂O₆ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 676.6±35.0 °C(Predicted) | |
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a chiral building block for the preparation of complex bioactive peptides. Its stereochemistry allows for precise control in the formation of specific peptide sequences, particularly in the development of pharmaceuticals targeting neurological and metabolic disorders. The presence of orthogonal protecting groups—Fmoc and Boc—enables selective deprotection and stepwise assembly in solid-phase peptide synthesis. It is especially valuable in the construction of peptidomimetics and constrained peptides where conformational rigidity is required for biological activity.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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100mg | 10-20 days | ฿4,950.00 |
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1g | 10-20 days | ฿22,570.00 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((R)-1-(tert-butoxycarbonyl)piperidin-3-yl)propanoic acid
Widely used in peptide synthesis, this compound serves as a chiral building block for the preparation of complex bioactive peptides. Its stereochemistry allows for precise control in the formation of specific peptide sequences, particularly in the development of pharmaceuticals targeting neurological and metabolic disorders. The presence of orthogonal protecting groups—Fmoc and Boc—enables selective deprotection and stepwise assembly in solid-phase peptide synthesis. It is especially valuable in the construction of peptidomimetics and constrained peptides where conformational rigidity is required for biological activity.
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