Z-D-Asn(Trt)-OH

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Reagent Code: #52355
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CAS Number 200259-87-6

science Other reagents with same CAS 200259-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 508.56 g/mol
Formula C₃₁H₂₈N₂O₅
badge Registry Numbers
MDL Number MFCD00237334
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used in peptide synthesis as a protected form of D-asparagine, ensuring selective reactions during the construction of peptide chains. It helps prevent unwanted side reactions by protecting the alpha-amino, carboxyl, and side chain groups. Commonly applied in the production of complex peptides for pharmaceutical research and drug development. The Z (Cbz) group protects the alpha-amino function, while the trityl (Trt) group protects the asparagine side chain amide, providing stability under acidic conditions and making it suitable for solid-phase peptide synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿441.00
inventory 5g
10-20 days ฿882.00

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Z-D-Asn(Trt)-OH
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Used in peptide synthesis as a protected form of D-asparagine, ensuring selective reactions during the construction of peptide chains. It helps prevent unwanted side reactions by protecting the alpha-amino, carboxyl, and side chain groups. Commonly applied in the production of complex peptides for pharmaceutical research and drug development. The Z (Cbz) group protects the alpha-amino function, while the trityl (Trt) group protects the asparagine side chain amide, providing stability under acidic conditions
Used in peptide synthesis as a protected form of D-asparagine, ensuring selective reactions during the construction of peptide chains. It helps prevent unwanted side reactions by protecting the alpha-amino, carboxyl, and side chain groups. Commonly applied in the production of complex peptides for pharmaceutical research and drug development. The Z (Cbz) group protects the alpha-amino function, while the trityl (Trt) group protects the asparagine side chain amide, providing stability under acidic conditions and making it suitable for solid-phase peptide synthesis.
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