(S)-6-(((Benzyloxy)carbonyl)amino)-2-(methylamino)hexanoic acid

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Reagent Code: #236434
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CAS Number 201016-22-0

science Other reagents with same CAS 201016-22-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.346 g/mol
Formula C₁₅H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD00672352
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex bioactive peptides. The benzyloxycarbonyl (Cbz) group serves as an amine protecting group, allowing selective deprotection and coupling in solid-phase or solution-phase peptide assembly. The stereochemistry (S-configuration) ensures proper chiral integrity in the final peptide product, which is critical for biological activity. Commonly employed in the synthesis of protease inhibitors and other pharmaceutical agents where precise amino acid sequence and configuration are required. Also utilized as an intermediate in the production of antibiotics and enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,070.00
inventory 250mg
10-20 days ฿19,780.00
inventory 1g
10-20 days ฿62,260.00

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(S)-6-(((Benzyloxy)carbonyl)amino)-2-(methylamino)hexanoic acid
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Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex bioactive peptides. The benzyloxycarbonyl (Cbz) group serves as an amine protecting group, allowing selective deprotection and coupling in solid-phase or solution-phase peptide assembly. The stereochemistry (S-configuration) ensures proper chiral integrity in the final peptide product, which is critical for biological activity. Commonly employed in the synthesis of protease inhibitors and other phar

Used in peptide synthesis as a protected amino acid derivative, particularly in the preparation of complex bioactive peptides. The benzyloxycarbonyl (Cbz) group serves as an amine protecting group, allowing selective deprotection and coupling in solid-phase or solution-phase peptide assembly. The stereochemistry (S-configuration) ensures proper chiral integrity in the final peptide product, which is critical for biological activity. Commonly employed in the synthesis of protease inhibitors and other pharmaceutical agents where precise amino acid sequence and configuration are required. Also utilized as an intermediate in the production of antibiotics and enzyme inhibitors.

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