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

≥95%

Reagent Code: #37422
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CAS Number 1217820-78-4

science Other reagents with same CAS 1217820-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 423.41 g/mol
Formula C₂₄H₁₉F₂NO₄
badge Registry Numbers
MDL Number MFCD07371997
thermostat Physical Properties
Boiling Point 618.5±55.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. Its structure includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used to shield the amino group during the synthesis process. The presence of the 2,4-difluorophenyl group in the molecule makes it particularly useful in the development of peptides with specific binding properties or biological activities. It is often employed in the production of peptide-based drugs, where precise control over the sequence and structure of the peptide is crucial. Additionally, its application extends to research in medicinal chemistry, where it is used to study the interactions of peptides with various biological targets.

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Test Parameter Specification
Appearance White to Off-White Powder or Crystals
Purity (%) 95.0-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,374.00
inventory 250mg
10-20 days ฿8,748.00

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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2,4-difluorophenyl)propanoic acid
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This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. Its structure includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used to shield the amino group during the synthesis process. The presence of the 2,4-difluorophenyl group in the molecule makes it particularly useful in the development of peptides with specific binding properties or biological activities. It is often employed in the production of peptide-

This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. Its structure includes a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used to shield the amino group during the synthesis process. The presence of the 2,4-difluorophenyl group in the molecule makes it particularly useful in the development of peptides with specific binding properties or biological activities. It is often employed in the production of peptide-based drugs, where precise control over the sequence and structure of the peptide is crucial. Additionally, its application extends to research in medicinal chemistry, where it is used to study the interactions of peptides with various biological targets.

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