94073-86-6

Basic information

• Product Name: Benzene, [1-(methoxymethoxy)ethyl]-
• CAS NO: 94073-86-6
• Molecular Formula: C10H14O2
• Molecular Weight: 166.22
• Mol File: 94073-86-6.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Benzene, [1-(methoxymethoxy)ethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [1-(methoxymethoxy)ethyl]-(94073-86-6)
• EPA Substance Registry System: Benzene, [1-(methoxymethoxy)ethyl]-(94073-86-6)

Safety Data

• Hazardous Substances Data: 94073-86-6(Hazardous Substances Data)

Upstream product

• 123294-04-2 Tributyl-(1-methoxymethoxy-1-phenyl-ethyl)-stannane 
• 98-85-1 1-Phenylethanol 
• 105104-40-3 Okahara's reagent 
• 109-87-5 Dimethoxymethane 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 10340-49-5 4-phenyl-1-pentene 
• 1195777-04-8 C₁₀H₁₃⁽²⁾HO₂ 
• 1201652-02-9 (3-(1-phenylethoxy)prop-1-yn-1-yl)benzene 
• 10604-60-1 (1-iodoethyl)benzene 
• 620-05-3 iodomethylbenzene 
• 100-39-0 benzyl bromide 
• 585-71-7 (1-bromoethyl)benzne 
• 140-29-4 phenylacetonitrile 
• 1823-91-2 1-phenylethyl cyanide 
• 32366-25-9 1-azidoethylbenzene 
• 98-85-1 1-Phenylethanol 
• 14856-75-8 1-phenyl-1-trimethylsilyloxyethane 
• 93-92-5 1-phenylethyl acetate 
• 873-76-7 para-Chlorobenzyl alcohol 

Relevant articles and documents

P4VPy–CuO nanoparticles as a novel and reusable catalyst: application at the protection of alcohols, phenols and amines

P4VPy–CuO nanoparticles were synthesized using ultrasound irradiations. Relevant properties of the synthesized nanoparticles were investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Fourier transform infrared spectroscopy. After identification, the prepared reagent was used for the promotion of different types of protection reactions of alcohols, phenols and amines. Easy workup, short reaction times, excellent yields, relatively low cost and reusability of the catalyst are the striking features of the reported methods.

[InCl4]: An efficient catalyst-medium for alkoxymethylation of alcohols and their interconversion to acetates and TMS-ethers

A simple, green and chemoselective method for methoxymethylation and ethoxymethylation of primary and secondary alcohols using a Lewis acidic room temperature ionic liquid, [C4mim][InCl4], as catalyst and reaction medium under ambient temperature, microwave and ultrasonic irradiations is reported. In this catalytic system, the corresponding MOM-and EOM-ethers are obtained in excellent yields and in short reaction times. Furthermore, this catalytic system was used for mild and efficient transformations of these protected alcohols to their corresponding acetates and trimethylsilyl ethers under thermal conditions and microwave and ultrasonic irradiations.

High-valent [SnIV(Br8TPP)(OTf)2] as a highly efficient and reusable catalyst for selective methoxymethylation of alcohols and phenols: The effect of substituted bromines on the catalytic activity

High-valent tin(IV)octabromotetraphenylporphyrinato trifluoromethanesulfonate, [SnIV(Br8TPP)(OTf)2], was used for selective methoxymethylation of alcohols and phenols with formaldehyde dimethyl acetal (FDMA) at room temper