6-[[(Benzyloxy)Carbonyl]Amino]Hexanoic Acid Tert-Butyl Ester

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Reagent Code: #153926
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CAS Number 158141-67-4

science Other reagents with same CAS 158141-67-4

blur_circular Chemical Specifications

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Weight 321.41 g/mol
Formula C₁₈H₂₇NO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a protected amino acid derivative in peptide synthesis, enabling selective coupling and preventing unwanted side reactions. The tert-butyl ester and benzyloxycarbonyl (Cbz) protecting groups allow stepwise assembly of peptides with high purity. Commonly employed in solid-phase and solution-phase synthesis of bioactive peptides, pharmaceuticals, and research compounds where controlled deprotection is required. Also utilized in the preparation of peptide-based prodrugs and conjugates due to its stability under various reaction conditions and ease of removal under mild acidic or hydrogenolytic conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,860.00

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6-[[(Benzyloxy)Carbonyl]Amino]Hexanoic Acid Tert-Butyl Ester
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Used as a protected amino acid derivative in peptide synthesis, enabling selective coupling and preventing unwanted side reactions. The tert-butyl ester and benzyloxycarbonyl (Cbz) protecting groups allow stepwise assembly of peptides with high purity. Commonly employed in solid-phase and solution-phase synthesis of bioactive peptides, pharmaceuticals, and research compounds where controlled deprotection is required. Also utilized in the preparation of peptide-based prodrugs and conjugates due to its sta

Used as a protected amino acid derivative in peptide synthesis, enabling selective coupling and preventing unwanted side reactions. The tert-butyl ester and benzyloxycarbonyl (Cbz) protecting groups allow stepwise assembly of peptides with high purity. Commonly employed in solid-phase and solution-phase synthesis of bioactive peptides, pharmaceuticals, and research compounds where controlled deprotection is required. Also utilized in the preparation of peptide-based prodrugs and conjugates due to its stability under various reaction conditions and ease of removal under mild acidic or hydrogenolytic conditions.

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