2-Amino-3-(4-fluoro-1H-indol-3-yl)propanoic acid

97%

Reagent Code: #42576
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CAS Number 25631-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.22 g/mol
Formula C₁₁H₁₁FN₂O₂
badge Registry Numbers
MDL Number MFCD00039689
thermostat Physical Properties
Boiling Point 450.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, protected from light and stored in an inert gas

description Product Description

This compound is primarily utilized in biochemical research due to its structural similarity to tryptophan, a crucial amino acid. It is often employed in studies investigating the role of fluorine substitution in biological systems, particularly in enzyme interactions and receptor binding. Its fluorinated indole structure makes it valuable for probing metabolic pathways and designing fluorinated analogs of bioactive molecules. Additionally, it serves as a building block in the synthesis of novel peptides and pharmaceuticals, especially those targeting neurological disorders or cancer, where fluorine incorporation can enhance stability and bioavailability. Its unique properties also make it a candidate for fluorescence labeling in imaging and diagnostic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,506.00
inventory 250mg
10-20 days ฿13,122.00
inventory 1g
10-20 days ฿20,889.00
2-Amino-3-(4-fluoro-1H-indol-3-yl)propanoic acid
This compound is primarily utilized in biochemical research due to its structural similarity to tryptophan, a crucial amino acid. It is often employed in studies investigating the role of fluorine substitution in biological systems, particularly in enzyme interactions and receptor binding. Its fluorinated indole structure makes it valuable for probing metabolic pathways and designing fluorinated analogs of bioactive molecules. Additionally, it serves as a building block in the synthesis of novel peptides and pharmaceuticals, especially those targeting neurological disorders or cancer, where fluorine incorporation can enhance stability and bioavailability. Its unique properties also make it a candidate for fluorescence labeling in imaging and diagnostic applications.
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