3-(3-fluorobenzyl)-4-(3-fluoro-benzyloxy)benzaldehyde

95%

Reagent Code: #44289
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CAS Number 1000370-24-0

science Other reagents with same CAS 1000370-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.3473464 g/mol
Formula C₂₁H₁₆F₂O₂
badge Registry Numbers
MDL Number MFCD28502380
thermostat Physical Properties
Boiling Point 464.5±45.0 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.236±0.06 g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate for the development of more complex molecules. Its structure, featuring fluorinated benzyl groups, makes it valuable in the design of bioactive compounds, particularly in the field of medicinal chemistry. Researchers often employ it to create potential drug candidates targeting specific receptors or enzymes, leveraging the electron-withdrawing properties of fluorine to enhance binding affinity and metabolic stability. Additionally, it may be used in the synthesis of advanced materials, where its aromatic and fluorinated components contribute to unique electronic or structural properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,000.00
inventory 1g
10-20 days ฿50,436.00

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3-(3-fluorobenzyl)-4-(3-fluoro-benzyloxy)benzaldehyde
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This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate for the development of more complex molecules. Its structure, featuring fluorinated benzyl groups, makes it valuable in the design of bioactive compounds, particularly in the field of medicinal chemistry. Researchers often employ it to create potential drug candidates targeting specific receptors or enzymes, leveraging the electron-withdrawing properties of fluorine to enhance binding affinity and meta

This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate for the development of more complex molecules. Its structure, featuring fluorinated benzyl groups, makes it valuable in the design of bioactive compounds, particularly in the field of medicinal chemistry. Researchers often employ it to create potential drug candidates targeting specific receptors or enzymes, leveraging the electron-withdrawing properties of fluorine to enhance binding affinity and metabolic stability. Additionally, it may be used in the synthesis of advanced materials, where its aromatic and fluorinated components contribute to unique electronic or structural properties.

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