4-Bromo-1-chloro-2-(2-ethoxybenzyl)benzene

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Reagent Code: #152955
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CAS Number 1830346-16-1

science Other reagents with same CAS 1830346-16-1

blur_circular Chemical Specifications

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Weight 325.63 g/mol
Formula C₁₅H₁₄BrClO
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzyl scaffolds. Its halogen functionality allows for further transformations via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The ethoxybenzyl group contributes to lipophilicity and can influence binding affinity in drug design. It is also employed in research settings to prepare receptor ligands and enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,530.00
inventory 250mg
10-20 days ฿18,760.00
inventory 1g
10-20 days ฿65,240.00

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4-Bromo-1-chloro-2-(2-ethoxybenzyl)benzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzyl scaffolds. Its halogen functionality allows for further transformations via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The ethoxybenzyl group contributes to lipophilicity and can influence binding affinity in drug design. It is also employed in research settings to prepa

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzyl scaffolds. Its halogen functionality allows for further transformations via cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The ethoxybenzyl group contributes to lipophilicity and can influence binding affinity in drug design. It is also employed in research settings to prepare receptor ligands and enzyme inhibitors.

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