4-(1H-Pyrazol-4-yl)pyridine

97%

Reagent Code: #195921
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CAS Number 19959-71-8

science Other reagents with same CAS 19959-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.16 g/mol
Formula C₈H₇N₃
badge Registry Numbers
MDL Number MFCD00480339
inventory_2 Storage & Handling
Storage Inert gas, room temperature

description Product Description

Used in organic and coordination chemistry research as a ligand that coordinates effectively with transition metals, owing to its two nitrogen atoms from the pyridine and pyrazole rings, enabling the formation of specific and stable coordination compounds.

Commonly employed in the development of catalysts, particularly for carbon-carbon bond forming reactions such as Suzuki coupling or Heck reaction.

Additionally, it serves as a key starting material in the synthesis of biologically active compounds, including antimicrobials, antivirals, kinase inhibitors, and anti-inflammatory agents, due to its structural similarity to natural motifs found in biological systems.

It is also applied in materials science, such as in the creation of conductive polymers or organic materials for electronic devices like OLEDs or sensors, leveraging its excellent conductivity and electron transfer properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,960.00
inventory 1g
10-20 days ฿6,310.00
inventory 5g
10-20 days ฿26,070.00

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4-(1H-Pyrazol-4-yl)pyridine
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Used in organic and coordination chemistry research as a ligand that coordinates effectively with transition metals, owing to its two nitrogen atoms from the pyridine and pyrazole rings, enabling the formation of specific and stable coordination compounds.

Commonly employed in the development of catalysts, particularly for carbon-carbon bond forming reactions such as Suzuki coupling or Heck reaction.

Additionally, it serves as a key starting material in the synthesis of biologically active co

Used in organic and coordination chemistry research as a ligand that coordinates effectively with transition metals, owing to its two nitrogen atoms from the pyridine and pyrazole rings, enabling the formation of specific and stable coordination compounds.

Commonly employed in the development of catalysts, particularly for carbon-carbon bond forming reactions such as Suzuki coupling or Heck reaction.

Additionally, it serves as a key starting material in the synthesis of biologically active compounds, including antimicrobials, antivirals, kinase inhibitors, and anti-inflammatory agents, due to its structural similarity to natural motifs found in biological systems.

It is also applied in materials science, such as in the creation of conductive polymers or organic materials for electronic devices like OLEDs or sensors, leveraging its excellent conductivity and electron transfer properties.

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