216443-67-3

Basic information

• Product Name: 4-bromo-1-[(ethoxymethoxy)methyl]benzene
• Synonyms: 4-bromo-1-[(ethoxymethoxy)methyl]benzene
• CAS NO: 216443-67-3
• Molecular Weight: 245.116
• Mol File: 216443-67-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-bromo-1-[(ethoxymethoxy)methyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-1-[(ethoxymethoxy)methyl]benzene(216443-67-3)
• EPA Substance Registry System: 4-bromo-1-[(ethoxymethoxy)methyl]benzene(216443-67-3)

Safety Data

• Hazardous Substances Data: 216443-67-3(Hazardous Substances Data)

Upstream product

• 873-75-6 4-bromobenzenemethanol 
• 7087-68-5 N-ethyl-N,N-diisopropylamine 
• 3188-13-4 ethyl chloromethyl ether 
• 462-95-3 formaldehyde diethyl acetal 

Downstream Products

• 873-75-6 4-bromobenzenemethanol 
• 55883-45-9 4-bromobenzyliodide 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 16532-79-9 4-Bromophenylacetonitrile 
• 86605-93-8 (4-bromobenzyloxy)trimethylsilane 
• 21388-92-1 4-bromobenzyl acetate 
• 216443-68-4 4-ethoxymethoxymethylphenylboronic acid 

Relevant articles and documents

TIME TEMPERATURE INDICATOR BASED ON THIOALKYL AND THIOARYL SUBSTITUTED SPIROAROMATICS

The present invention relates to photochromic spiropyrans as active ingredients of Time-Temperature Indicators (TTIs), and to new spiropyrans per se. More particularly, the invention provides TTIs on the base of photochromic spiropyrans comprising alkylsu

[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.

Triaromatic compounds and pharmaceutical/cosmetic compositions comprised thereof

Novel pharmaceutically/cosmetically-active triaromatic compounds have the structural formula (I): and are useful for the treatment of a wide variety of disease states, whether human or veterinary, for example dermatological, rheumatic, respiratory, cardiovascular, bone and ophthalmological disorders, as well as for the treatment of mammalian skin and hair conditions/disorders.