Fmoc-Gly-Thr[Psi(Me,Me)Pro]-OH

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Reagent Code: #37009
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CAS Number 1262308-49-5

science Other reagents with same CAS 1262308-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 438.47 g/mol
Formula C₂₄H₂₆N₂O₆
badge Registry Numbers
MDL Number MFCD18427358
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for creating peptides with specific structural features, such as those involving pseudoproline dipeptides. The incorporation of pseudoproline residues helps to reduce aggregation and improve solubility during peptide chain assembly, making it valuable for synthesizing complex or difficult sequences. Its Fmoc-protected amino group ensures compatibility with Fmoc-based SPPS protocols, allowing for efficient deprotection and coupling steps. This chemical is especially useful in the production of peptides for research in biochemistry, drug development, and therapeutic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,790.00
inventory 1g
10-20 days ฿5,589.00

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Fmoc-Gly-Thr[Psi(Me,Me)Pro]-OH
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This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for creating peptides with specific structural features, such as those involving pseudoproline dipeptides. The incorporation of pseudoproline residues helps to reduce aggregation and improve solubility during peptide chain assembly, making it valuable for synthesizing complex or difficult sequences. Its Fmoc-protected amino group ensures compatibility with Fmoc

This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for creating peptides with specific structural features, such as those involving pseudoproline dipeptides. The incorporation of pseudoproline residues helps to reduce aggregation and improve solubility during peptide chain assembly, making it valuable for synthesizing complex or difficult sequences. Its Fmoc-protected amino group ensures compatibility with Fmoc-based SPPS protocols, allowing for efficient deprotection and coupling steps. This chemical is especially useful in the production of peptides for research in biochemistry, drug development, and therapeutic applications.

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