(R)-5-Amino-2-(((benzyloxy)carbonyl)(trityl)amino)-5-oxopentanoic acid

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Reagent Code: #37703
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CAS Number 200625-96-3

science Other reagents with same CAS 200625-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 522.59 g/mol
Formula C₃₂H₃₀N₂O₅
badge Registry Numbers
MDL Number MFCD00237348
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. Its structure, featuring a trityl group and a benzyloxycarbonyl (Cbz) protecting group, ensures selective deprotection during the synthesis of complex peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and maintain the integrity of the peptide chain. Additionally, its chiral nature allows for the production of enantiomerically pure peptides, which is crucial in pharmaceutical research and development. The compound’s stability and compatibility with various coupling reagents make it a reliable choice for synthesizing biologically active peptides and peptidomimetics.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,718.00
inventory 10g
10-20 days ฿7,767.00
inventory 5g
10-20 days ฿5,436.00

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(R)-5-Amino-2-(((benzyloxy)carbonyl)(trityl)amino)-5-oxopentanoic acid
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This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. Its structure, featuring a trityl group and a benzyloxycarbonyl (Cbz) protecting group, ensures selective deprotection during the synthesis of complex peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and maintain the integrity of the peptide chain. Additionally, its chiral nature allows for the production of enantiomerically pure peptides, which is

This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. Its structure, featuring a trityl group and a benzyloxycarbonyl (Cbz) protecting group, ensures selective deprotection during the synthesis of complex peptides. It is particularly valuable in solid-phase peptide synthesis (SPPS) to prevent unwanted side reactions and maintain the integrity of the peptide chain. Additionally, its chiral nature allows for the production of enantiomerically pure peptides, which is crucial in pharmaceutical research and development. The compound’s stability and compatibility with various coupling reagents make it a reliable choice for synthesizing biologically active peptides and peptidomimetics.

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