α-Fluoro-β-alanine

95%

Reagent Code: #111549
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CAS Number 3821-81-6

science Other reagents with same CAS 3821-81-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 107.0836 g/mol
Formula C₃H₆FNO₂
badge Registry Numbers
MDL Number MFCD00041324
thermostat Physical Properties
Boiling Point 264.5℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.302g/ml
Storage 2-8℃, dry

description Product Description

Used primarily in the synthesis of pharmaceuticals, particularly in the development of anticancer and antiviral drugs. It serves as a key intermediate in the production of fluorinated pyrimidines, which are essential in chemotherapy treatments. Additionally, it plays a role in biochemical research for studying enzyme mechanisms and metabolic pathways due to its fluorine substitution, which can mimic natural amino acids while altering reactivity.

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Test Parameter Specification
Appearance White to Beige
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,880.00
inventory 5mg
10-20 days ฿850.00
inventory 100mg
10-20 days ฿5,290.00
inventory 500mg
10-20 days ฿24,680.00

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α-Fluoro-β-alanine
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Used primarily in the synthesis of pharmaceuticals, particularly in the development of anticancer and antiviral drugs. It serves as a key intermediate in the production of fluorinated pyrimidines, which are essential in chemotherapy treatments. Additionally, it plays a role in biochemical research for studying enzyme mechanisms and metabolic pathways due to its fluorine substitution, which can mimic natural amino acids while altering reactivity.
Used primarily in the synthesis of pharmaceuticals, particularly in the development of anticancer and antiviral drugs. It serves as a key intermediate in the production of fluorinated pyrimidines, which are essential in chemotherapy treatments. Additionally, it plays a role in biochemical research for studying enzyme mechanisms and metabolic pathways due to its fluorine substitution, which can mimic natural amino acids while altering reactivity.
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