2-(Pyridin-2-yl)quinoline-4-carboxylic acid

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Reagent Code: #227614
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CAS Number 57882-27-6

science Other reagents with same CAS 57882-27-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.259 g/mol
Formula C₁₅H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD00224804
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It also serves as a ligand in coordination chemistry, forming complexes with metal ions that exhibit catalytic activity in organic transformations. Its structure supports fluorescence properties, making it useful in the design of sensors and optoelectronic materials. Additionally, it has been explored in antimicrobial and antiviral research due to its bioactive scaffold.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,430.00
inventory 5g
10-20 days ฿13,330.00
inventory 1g
10-20 days ฿2,850.00

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2-(Pyridin-2-yl)quinoline-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It also serves as a ligand in coordination chemistry, forming complexes with metal ions that exhibit catalytic activity in organic transformations. Its structure supports fluorescence properties, making it useful in the design of sensors and optoelectronic materials. Additionally, it has been explored in antimicrobial and antiviral research due to its bioacti

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It also serves as a ligand in coordination chemistry, forming complexes with metal ions that exhibit catalytic activity in organic transformations. Its structure supports fluorescence properties, making it useful in the design of sensors and optoelectronic materials. Additionally, it has been explored in antimicrobial and antiviral research due to its bioactive scaffold.

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