4-(4-Amino-3-fluorophenoxy)-N-methylpicolinamide

>95%

Reagent Code: #66338
label
Alias 4-(4-amino-3-fluorophenoxy)pyridine-2-carboxylic acid methylamine; 4-(4-amino-3-fluorophenoxy)-N-methyl-2-pyridinecarboxamide;
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CAS Number 757251-39-1

science Other reagents with same CAS 757251-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.25 g/mol
Formula C₁₃H₁₂FN₃O₂
badge Registry Numbers
MDL Number MFCD09033852
thermostat Physical Properties
Boiling Point 459.8ºC at 760 mmHg
inventory_2 Storage & Handling
Density 1.305g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of tyrosine kinase inhibitors, which are crucial in targeted cancer therapies. By acting on specific signaling pathways, these inhibitors can effectively halt the proliferation of cancer cells. Additionally, the presence of both amino and fluorine groups in the molecule enhances its binding affinity to biological targets, making it a versatile building block for designing drugs with improved efficacy and selectivity. Researchers also explore its potential in creating compounds for treating inflammatory diseases and other conditions where kinase modulation is beneficial.

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Test Parameter Specification
Purity 95-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1 g
10-20 days ฿1,980.00

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4-(4-Amino-3-fluorophenoxy)-N-methylpicolinamide
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This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of tyrosine kinase inhibitors, which are crucial in targeted cancer therapies. By acting on specific signaling pathways, these inhibitors can effectively halt the proliferation of cancer cells. Additionally, the presence of both amino and fluorine groups in the molecule enhances its binding affinity to biological targets, making it a versatile building block for designing drugs with improved efficacy and selectivity. Researchers also explore its potential in creating compounds for treating inflammatory diseases and other conditions where kinase modulation is beneficial.
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