1020186-15-5

Basic information

• Product Name: 1-(((1-ethynylcyclohexyl)oxy)methyl)-4-methoxybenzene
• Synonyms: 1-(((1-ethynylcyclohexyl)oxy)methyl)-4-methoxybenzene
• CAS NO: 1020186-15-5
• Molecular Weight: 244.334
• Mol File: 1020186-15-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(((1-ethynylcyclohexyl)oxy)methyl)-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(((1-ethynylcyclohexyl)oxy)methyl)-4-methoxybenzene(1020186-15-5)
• EPA Substance Registry System: 1-(((1-ethynylcyclohexyl)oxy)methyl)-4-methoxybenzene(1020186-15-5)

Safety Data

• Hazardous Substances Data: 1020186-15-5(Hazardous Substances Data)

Upstream product

• 937184-70-8 2-(4-methoxybenzyloxy)-4-methylquinoline 
• 78-27-3 1-Ethynylcyclohexan-1-ol 
• 824-94-2 p-methoxybenzyl chloride 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 78-27-3 1-Ethynylcyclohexan-1-ol 

Relevant articles and documents

Oxidative Deprotection of p-Methoxybenzyl Ethers via Metal-Free Photoredox Catalysis

An efficient and greener deprotection method for p-methoxybenzyl (PMB) ethers using a metal-free visible light photoredox catalyst and air and ammonium persulfate as the terminal oxidants is presented. Various functional groups and protecting groups were tolerated in the developed method to achieve good to excellent yields in short reaction times. Significantly, the developed method was compatible with PMB ethers derived from primary, secondary, and tertiary alcohols and a gram-scale reaction. Mechanistic studies support a proposed reaction mechanism that involves single electron oxidation of the PMB ether.

A simple and an efficient indium trichloride catalyzed benzyl etherification

An efficient method has been developed for the synthesis of benzyl ethers of alkyl, allyl and propargyl alchols by simple, direct coupling of alcohols in the presence of catalytic amount of L1C13 under solvent-free condition.