(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((R)-1-(tert-butoxycarbonyl)piperidin-3-yl)propanoic acid

95%

Reagent Code: #232426
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CAS Number 1251904-14-9

science Other reagents with same CAS 1251904-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 494.59 g/mol
Formula C₂₈H₃₄N₂O₆
thermostat Physical Properties
Boiling Point 676.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,950.00
1g
10-20 days ฿22,570.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((R)-1-(tert-butoxycarbonyl)piperidin-3-yl)propanoic acid
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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 cons

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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