(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid

98%

Reagent Code: #104241
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CAS Number 511272-36-9

science Other reagents with same CAS 511272-36-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 403.43 g/mol
Formula C₂₄H₂₁NO₅
badge Registry Numbers
MDL Number MFCD03428017
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in peptide synthesis as a building block for creating complex peptide structures. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. This allows for controlled and sequential peptide chain elongation in solid-phase peptide synthesis (SPPS). The hydroxyl group on the phenyl ring provides an additional site for further functionalization or conjugation, making it valuable in the development of peptide-based drugs, biomaterials, or research tools. Its application is particularly significant in medicinal chemistry and biochemistry for synthesizing peptides with specific biological activities or targeting properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,268.00
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoic acid
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This chemical is primarily used in peptide synthesis as a building block for creating complex peptide structures. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. This allows for controlled and sequential peptide chain elongation in solid-phase peptide synthesis (SPPS). The hydroxyl group on the phenyl ring provides an additional site for further functionalization or conjugation, making it valuable in t

This chemical is primarily used in peptide synthesis as a building block for creating complex peptide structures. It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. This allows for controlled and sequential peptide chain elongation in solid-phase peptide synthesis (SPPS). The hydroxyl group on the phenyl ring provides an additional site for further functionalization or conjugation, making it valuable in the development of peptide-based drugs, biomaterials, or research tools. Its application is particularly significant in medicinal chemistry and biochemistry for synthesizing peptides with specific biological activities or targeting properties.

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