N-(1-Naphthalenesulfonyl)-L-phenylalanyl Chloride

≥98%

Reagent Code: #96194
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CAS Number 146864-62-2

science Other reagents with same CAS 146864-62-2

blur_circular Chemical Specifications

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Weight 373.85 g/mol
Formula C₁₉H₁₆ClNO₃S
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MDL Number MFCD00191468
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description Product Description

This compound is primarily utilized in peptide synthesis as a reagent for introducing the phenylalanine residue into peptide chains. Its naphthalenesulfonyl group acts as a protecting group, ensuring selective reactions during the synthesis process. It is particularly valuable in solid-phase peptide synthesis, where it helps in constructing complex peptides with high precision. Additionally, it is employed in biochemical research to study enzyme-substrate interactions and to modify peptides for functional analysis. Its stability and reactivity make it a useful tool in organic chemistry laboratories for designing and synthesizing novel peptide-based compounds.

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inventory 1g
10-20 days ฿3,180.00
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N-(1-Naphthalenesulfonyl)-L-phenylalanyl Chloride
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This compound is primarily utilized in peptide synthesis as a reagent for introducing the phenylalanine residue into peptide chains. Its naphthalenesulfonyl group acts as a protecting group, ensuring selective reactions during the synthesis process. It is particularly valuable in solid-phase peptide synthesis, where it helps in constructing complex peptides with high precision. Additionally, it is employed in biochemical research to study enzyme-substrate interactions and to modify peptides for functiona

This compound is primarily utilized in peptide synthesis as a reagent for introducing the phenylalanine residue into peptide chains. Its naphthalenesulfonyl group acts as a protecting group, ensuring selective reactions during the synthesis process. It is particularly valuable in solid-phase peptide synthesis, where it helps in constructing complex peptides with high precision. Additionally, it is employed in biochemical research to study enzyme-substrate interactions and to modify peptides for functional analysis. Its stability and reactivity make it a useful tool in organic chemistry laboratories for designing and synthesizing novel peptide-based compounds.

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