1-(4-(Benzyloxy)phenyl)-2-bromoethanone

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Reagent Code: #145724
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CAS Number 4254-67-5

science Other reagents with same CAS 4254-67-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.17 g/mol
Formula C₁₅H₁₃BrO₂
thermostat Physical Properties
Boiling Point 419.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of beta-blockers and other cardiovascular drugs. It serves as a building block for introducing bromoethyl functional groups into more complex molecules. Commonly employed in organic synthesis for constructing heterocyclic compounds and in the development of kinase inhibitors. Its benzyloxy-phenyl structure allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry research and drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿4,130.00

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1-(4-(Benzyloxy)phenyl)-2-bromoethanone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of beta-blockers and other cardiovascular drugs. It serves as a building block for introducing bromoethyl functional groups into more complex molecules. Commonly employed in organic synthesis for constructing heterocyclic compounds and in the development of kinase inhibitors. Its benzyloxy-phenyl structure allows for further functionalization through cross-coupling reactions, making it valuable in medicinal ch

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of beta-blockers and other cardiovascular drugs. It serves as a building block for introducing bromoethyl functional groups into more complex molecules. Commonly employed in organic synthesis for constructing heterocyclic compounds and in the development of kinase inhibitors. Its benzyloxy-phenyl structure allows for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry research and drug discovery.

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