(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid

98%

Reagent Code: #38023
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CAS Number 204058-25-3

science Other reagents with same CAS 204058-25-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 494.5800 g/mol
Formula C₂₈H₃₄N₂O₆
badge Registry Numbers
MDL Number MFCD01321423
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptides and proteins, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butoxycarbonyl (Boc) group shields the piperidine nitrogen, ensuring selective reactions during peptide chain assembly. Its structure allows for the introduction of piperidine-containing motifs into peptides, which are often explored in drug development for their potential bioactivity. After synthesis, the protecting groups can be removed under specific conditions to yield the desired peptide sequence. This compound is particularly valuable in pharmaceutical research for creating peptide-based therapeutics and studying biological interactions.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 97.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,438.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(1-(tert-butoxycarbonyl)piperidin-4-yl)propanoic acid
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This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptides and proteins, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butoxycarbonyl (Boc) group shields the piperidine nitrogen, ensuring selective reactions during peptide chain assembly. Its structure allows for the introduction of piperidine-containing motifs into pept

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptides and proteins, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group protects the amino group, while the tert-butoxycarbonyl (Boc) group shields the piperidine nitrogen, ensuring selective reactions during peptide chain assembly. Its structure allows for the introduction of piperidine-containing motifs into peptides, which are often explored in drug development for their potential bioactivity. After synthesis, the protecting groups can be removed under specific conditions to yield the desired peptide sequence. This compound is particularly valuable in pharmaceutical research for creating peptide-based therapeutics and studying biological interactions.

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