(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(2,3-dihydro-1H-inden-2-yl)acetic acid

95%

Reagent Code: #38012
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CAS Number 205526-39-2

science Other reagents with same CAS 205526-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 413.4700 g/mol
Formula C₂₆H₂₃NO₄
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MDL Number MFCD00672561
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key building block for the creation of complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis (SPPS), as it allows for the selective deprotection of amino acids during the stepwise assembly of peptides. The 2,3-dihydro-1H-inden-2-yl (indane) moiety in its structure can contribute to the stabilization of peptide conformations or interactions with biological targets. It is often employed in the development of peptide-based pharmaceuticals, where precise control over amino acid sequence and structure is critical. Additionally, it may be used in research applications to study peptide-protein interactions or to design novel bioactive compounds with potential therapeutic applications.

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inventory 100mg
10-20 days ฿5,337.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(2,3-dihydro-1H-inden-2-yl)acetic acid
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This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key building block for the creation of complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis (SPPS), as it allows for the selective deprotection of amino acids during the stepwise assembly of peptides. The 2,3-dihydro-1H-inden-2-yl (indane) moiety in its structure can contribute to the stabilization of peptide conformations or int

This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key building block for the creation of complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis (SPPS), as it allows for the selective deprotection of amino acids during the stepwise assembly of peptides. The 2,3-dihydro-1H-inden-2-yl (indane) moiety in its structure can contribute to the stabilization of peptide conformations or interactions with biological targets. It is often employed in the development of peptide-based pharmaceuticals, where precise control over amino acid sequence and structure is critical. Additionally, it may be used in research applications to study peptide-protein interactions or to design novel bioactive compounds with potential therapeutic applications.

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