(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(((benzyloxy)carbonyl)amino)propanoic acid

98%

Reagent Code: #37420
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CAS Number 387824-80-8

science Other reagents with same CAS 387824-80-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 460.4800 g/mol
Formula C₂₆H₂₄N₂O₆
badge Registry Numbers
MDL Number MFCD02684373
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the fluorenylmethoxycarbonyl (Fmoc) and benzyloxycarbonyl (Cbz) protecting groups. The Fmoc group protects the amino group, allowing selective deprotection under mild basic conditions, while the Cbz group provides additional protection for side-chain functionalities. This dual protection strategy enables the precise and sequential assembly of peptide chains, ensuring high purity and yield. It is commonly employed in the synthesis of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and compatibility with various coupling reagents make it a versatile tool in organic and medicinal chemistry.

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

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿702.00

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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(((benzyloxy)carbonyl)amino)propanoic acid
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This compound is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the fluorenylmethoxycarbonyl (Fmoc) and benzyloxycarbonyl (Cbz) protecting groups. The Fmoc group protects the amino group, allowing selective deprotection under mild basic conditions, while the Cbz group provides additional protection for side-chain functionalities. This dual protection strategy

This compound is primarily used in the field of peptide synthesis, where it serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the fluorenylmethoxycarbonyl (Fmoc) and benzyloxycarbonyl (Cbz) protecting groups. The Fmoc group protects the amino group, allowing selective deprotection under mild basic conditions, while the Cbz group provides additional protection for side-chain functionalities. This dual protection strategy enables the precise and sequential assembly of peptide chains, ensuring high purity and yield. It is commonly employed in the synthesis of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and compatibility with various coupling reagents make it a versatile tool in organic and medicinal chemistry.

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