72293-97-1

Basic information

• Product Name: Ethanone, 1-[4-[(4-methoxyphenyl)methoxy]phenyl]-
• Synonyms: 4-(4-methoxybenzyloxy)acetophenone;1-[4-(4-methoxy-benzyloxy)phenyl]ethanone;4-(4-Methoxybenzyloxy)acetophenon;1-[4-[(4-methoxyphenyl)-methoxy]phenyl]ethanone;1-{4-[(4-methoxyphenyl)methoxy]phenyl}ethan-1-one;Ethanone,1-[4-[(4-methoxyphenyl)methoxy]phenyl]
• CAS NO: 72293-97-1
• Molecular Formula: C16H16O3
• Molecular Weight: 256.301
• Mol File: 72293-97-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[4-[(4-methoxyphenyl)methoxy]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[4-[(4-methoxyphenyl)methoxy]phenyl]-(72293-97-1)
• EPA Substance Registry System: Ethanone, 1-[4-[(4-methoxyphenyl)methoxy]phenyl]-(72293-97-1)

Safety Data

• Hazardous Substances Data: 72293-97-1(Hazardous Substances Data)

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 99-93-4 4-Hydroxyacetophenone 
• 2746-25-0 p-Methoxybenzyl bromide 
• 104-93-8 p-methylanizole 

Downstream Products

• 99-93-4 4-Hydroxyacetophenone 
• 1413765-63-5 4-hydroxy-4’-(4-methoxybenzyloxy)-2,6-dimethoxychalcone 
• 1413765-67-9 3-(4-hydroxy-2,6-dimethoxyphenyl)-1-[4-(4-methoxybenzyloxy)phenyl]-1-propanone 
• 1377901-51-3 C₂₂H₃₀O₃Si 
• 1164381-20-7 2-(dimethylaminomethyl)-1-[4'-(4''-methoxybenzyloxy)phenyl]-prop-2-en-1-one hydrochloride 
• 79615-62-6 4-[4-(4-Methoxy-benzyloxy)-phenyl]-thiazol-2-ylamine; hydrochloride 
• 123-07-9 4-Ethylphenol 

Relevant articles and documents

Facile and selective deprotection of PMB ethers and esters using oxalyl chloride

Oxalyl chloride, (0.5 equiv) was found to cleave the PMB group from alkyl, aryl PMB ethers, and esters to give corresponding alcohol and acid in good yields. This method offers simple and efficient protocol for the selective deprotection of PMB ether and ester in DCE at ambient temperature.

A New, Convenient Reductive Procedure for the Deprotection of 4-Methoxybenzyl (MPM) Ethers to Alcohols

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Synthesis of several benzyloxphenyl derivatives with local anesthetic activity (author's transl)

Several 2- and 4-benzyloxy- and 4-(2'- and 4'-substituted) benzyloxy-beta-substituted amino-propiophenones, some of the corresponding alcohols, some 4-benzyloxy-alpha-substituted amino-acetophenones were synthetised and tested for their pharmacological activity.