ABZ-GLY-OH HCL

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Reagent Code: #124519
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CAS Number 256657-23-5

science Other reagents with same CAS 256657-23-5

blur_circular Chemical Specifications

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Weight 230.65 g/mol
Formula C₉H₁₁ClN₂O₃
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description Product Description

ABZ-GLY-OH HCl is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing larger peptide chains, where the ABZ (aminobenzoic acid) group acts as a protective group to prevent unwanted reactions during the synthesis process. This compound is particularly useful in solid-phase peptide synthesis (SPPS), where it helps ensure the correct sequence of amino acids is maintained. Additionally, it finds applications in research and development for creating peptide-based drugs, biomaterials, and bioactive compounds. Its stability and ease of deprotection make it a valuable tool in organic and medicinal chemistry laboratories.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿22,509.00
inventory 1g
10-20 days ฿14,499.00

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ABZ-GLY-OH HCL
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ABZ-GLY-OH HCl is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing larger peptide chains, where the ABZ (aminobenzoic acid) group acts as a protective group to prevent unwanted reactions during the synthesis process. This compound is particularly useful in solid-phase peptide synthesis (SPPS), where it helps ensure the correct sequence of amino acids is maintained. Additionally, it finds applications in research and development for c

ABZ-GLY-OH HCl is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing larger peptide chains, where the ABZ (aminobenzoic acid) group acts as a protective group to prevent unwanted reactions during the synthesis process. This compound is particularly useful in solid-phase peptide synthesis (SPPS), where it helps ensure the correct sequence of amino acids is maintained. Additionally, it finds applications in research and development for creating peptide-based drugs, biomaterials, and bioactive compounds. Its stability and ease of deprotection make it a valuable tool in organic and medicinal chemistry laboratories.

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