Z-D-Leu-onp

≥95%

Reagent Code: #105839
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CAS Number 52235-17-3

science Other reagents with same CAS 52235-17-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.40 g/mol
Formula C₂₀H₂₂N₂O₆
badge Registry Numbers
MDL Number MFCD00153338
thermostat Physical Properties
Boiling Point 561.3±45.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Z-D-Leu-onp is a protected and activated derivative of D-leucine, featuring a benzyloxycarbonyl (Z) group on the amino function and a p-nitrophenyl (ONp) ester on the carboxyl group. It serves as a key building block in peptide synthesis, particularly for incorporating D-leucine residues. The active ester facilitates efficient coupling reactions, while the Z-protection prevents unwanted side reactions during peptide bond formation. It is commonly used in solid-phase peptide synthesis (SPPS) to enable selective deprotection and high-yield coupling, ensuring the production of complex peptides with high purity and stereochemical specificity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,130.00

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Z-D-Leu-onp
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Z-D-Leu-onp is a protected and activated derivative of D-leucine, featuring a benzyloxycarbonyl (Z) group on the amino function and a p-nitrophenyl (ONp) ester on the carboxyl group. It serves as a key building block in peptide synthesis, particularly for incorporating D-leucine residues. The active ester facilitates efficient coupling reactions, while the Z-protection prevents unwanted side reactions during peptide bond formation. It is commonly used in solid-phase peptide synthesis (SPPS) to enable sel

Z-D-Leu-onp is a protected and activated derivative of D-leucine, featuring a benzyloxycarbonyl (Z) group on the amino function and a p-nitrophenyl (ONp) ester on the carboxyl group. It serves as a key building block in peptide synthesis, particularly for incorporating D-leucine residues. The active ester facilitates efficient coupling reactions, while the Z-protection prevents unwanted side reactions during peptide bond formation. It is commonly used in solid-phase peptide synthesis (SPPS) to enable selective deprotection and high-yield coupling, ensuring the production of complex peptides with high purity and stereochemical specificity.

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