2-Amino-3-(2,6-difluorophenyl)propanoic acid

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Reagent Code: #42110
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CAS Number 32133-39-4

science Other reagents with same CAS 32133-39-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.17 g/mol
Formula C₉H₉F₂NO₂
thermostat Physical Properties
Melting Point 256-257℃
Boiling Point 301.1±42.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.379 g/cm3
Storage 2-8°C, dry, airtight

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of pharmaceuticals. It is often employed in the development of drugs targeting neurological disorders due to its structural similarity to certain amino acids that play a role in brain function. Additionally, it serves as a building block in the creation of peptide-based therapies, where its unique fluorinated aromatic side chain can enhance binding affinity and stability. Researchers also explore its potential in designing enzyme inhibitors, particularly for enzymes involved in metabolic pathways or disease mechanisms. Its fluorinated structure makes it valuable in the study of fluorine's impact on drug efficacy and pharmacokinetics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,852.00
inventory 1g
10-20 days ฿7,812.00
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2-Amino-3-(2,6-difluorophenyl)propanoic acid
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of pharmaceuticals. It is often employed in the development of drugs targeting neurological disorders due to its structural similarity to certain amino acids that play a role in brain function. Additionally, it serves as a building block in the creation of peptide-based therapies, where its unique fluorinated aromatic side chain can enhance binding affinity and stability. Researchers also explor

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of pharmaceuticals. It is often employed in the development of drugs targeting neurological disorders due to its structural similarity to certain amino acids that play a role in brain function. Additionally, it serves as a building block in the creation of peptide-based therapies, where its unique fluorinated aromatic side chain can enhance binding affinity and stability. Researchers also explore its potential in designing enzyme inhibitors, particularly for enzymes involved in metabolic pathways or disease mechanisms. Its fluorinated structure makes it valuable in the study of fluorine's impact on drug efficacy and pharmacokinetics.

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