(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid

95%

Reagent Code: #50305
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CAS Number 269396-54-5

science Other reagents with same CAS 269396-54-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 470.34 g/mol
Formula C₂₅H₂₁Cl₂NO₄
badge Registry Numbers
MDL Number MFCD01860947
thermostat Physical Properties
Boiling Point 672.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in solid-phase peptide synthesis (SPPS), where it serves as a protected amino acid derivative. Its fluorenylmethoxycarbonyl (Fmoc) group is crucial for temporary protection of the amino group during the synthesis process, ensuring selective reactions at specific sites. The presence of the dichlorophenyl group enhances its stability and influences its reactivity, making it suitable for constructing complex peptide sequences. It is particularly valuable in the production of pharmaceuticals and bioactive peptides, where precise control over molecular structure is essential. Additionally, its application extends to research and development in organic chemistry, aiding in the study of peptide interactions and functions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,871.00
inventory 250mg
10-20 days ฿4,869.00
inventory 1g
10-20 days ฿13,140.00

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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2,4-dichlorophenyl)butanoic acid
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This chemical is primarily utilized in solid-phase peptide synthesis (SPPS), where it serves as a protected amino acid derivative. Its fluorenylmethoxycarbonyl (Fmoc) group is crucial for temporary protection of the amino group during the synthesis process, ensuring selective reactions at specific sites. The presence of the dichlorophenyl group enhances its stability and influences its reactivity, making it suitable for constructing complex peptide sequences. It is particularly valuable in the production

This chemical is primarily utilized in solid-phase peptide synthesis (SPPS), where it serves as a protected amino acid derivative. Its fluorenylmethoxycarbonyl (Fmoc) group is crucial for temporary protection of the amino group during the synthesis process, ensuring selective reactions at specific sites. The presence of the dichlorophenyl group enhances its stability and influences its reactivity, making it suitable for constructing complex peptide sequences. It is particularly valuable in the production of pharmaceuticals and bioactive peptides, where precise control over molecular structure is essential. Additionally, its application extends to research and development in organic chemistry, aiding in the study of peptide interactions and functions.

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