5-(4-Fluorophenyl)-1H-pyrazole-3-carbaldehyde

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Reagent Code: #124350
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CAS Number 1107467-72-0

science Other reagents with same CAS 1107467-72-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.17 g/mol
Formula C₁₀H₇FN₂O
badge Registry Numbers
MDL Number MFCD10036215
thermostat Physical Properties
Boiling Point 414.7±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.337±0.06 g/cm3(Predicted)
Storage 2-8°C, inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a pyrazole ring, makes it a valuable building block for developing potential therapeutic agents. Researchers often employ it in the design and synthesis of compounds targeting enzymes or receptors, particularly in the development of anti-inflammatory, anticancer, and antimicrobial drugs. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. Its application extends to material science, where it can be used in the preparation of organic frameworks or as a precursor for advanced functional materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,364.00
inventory 1g
10-20 days ฿14,463.00
inventory 100mg
10-20 days ฿3,213.00

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5-(4-Fluorophenyl)-1H-pyrazole-3-carbaldehyde
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluorophenyl group and a pyrazole ring, makes it a valuable building block for developing potential therapeutic agents. Researchers often employ it in the design and synthesis of compounds targeting enzymes or receptors, particularly in the development of anti-inflammatory, anticancer, and antimicrobial drugs. Additionally, its aldehyde functional group allows for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. Its application extends to material science, where it can be used in the preparation of organic frameworks or as a precursor for advanced functional materials.
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