Fmoc-3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one

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Reagent Code: #75856
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CAS Number 215190-27-5

science Other reagents with same CAS 215190-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 511 g/mol
Formula C₃₀H₂₉N₃O₅
badge Registry Numbers
MDL Number MFCD00673795
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Fmoc-3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one is a specialized protected building block used in peptide synthesis. The Fmoc (Fluorenylmethyloxycarbonyl) group serves as a protecting group for the amino functionality of the spirocyclic scaffold, enabling its incorporation into peptides during solid-phase peptide synthesis (SPPS). This facilitates the stepwise assembly of peptides with precise control over sequence and structure. The unique spiro[4.5]decanone core provides conformational rigidity and specificity, making it particularly useful in developing peptide-based therapeutics, biomaterials, and targeted molecular agents. Its stability and mild deprotection conditions enhance its utility in complex organic synthesis and research on novel bioactive compounds, such as those interacting with enzymes or receptors.

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inventory 1g
10-20 days ฿19,647.00

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Fmoc-3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one
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Fmoc-3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one is a specialized protected building block used in peptide synthesis. The Fmoc (Fluorenylmethyloxycarbonyl) group serves as a protecting group for the amino functionality of the spirocyclic scaffold, enabling its incorporation into peptides during solid-phase peptide synthesis (SPPS). This facilitates the stepwise assembly of peptides with precise control over sequence and structure. The unique spiro[4.5]decanone core provides conformational

Fmoc-3-carboxymethyl-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one is a specialized protected building block used in peptide synthesis. The Fmoc (Fluorenylmethyloxycarbonyl) group serves as a protecting group for the amino functionality of the spirocyclic scaffold, enabling its incorporation into peptides during solid-phase peptide synthesis (SPPS). This facilitates the stepwise assembly of peptides with precise control over sequence and structure. The unique spiro[4.5]decanone core provides conformational rigidity and specificity, making it particularly useful in developing peptide-based therapeutics, biomaterials, and targeted molecular agents. Its stability and mild deprotection conditions enhance its utility in complex organic synthesis and research on novel bioactive compounds, such as those interacting with enzymes or receptors.

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