67856-23-9

Basic information

• Product Name: Ethanol, 2-[4-(phenylmethoxy)phenoxy]-
• CAS NO: 67856-23-9
• Molecular Formula: C15H16O3
• Molecular Weight: 244.29
• Mol File: 67856-23-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Ethanol, 2-[4-(phenylmethoxy)phenoxy]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanol, 2-[4-(phenylmethoxy)phenoxy]-(67856-23-9)
• EPA Substance Registry System: Ethanol, 2-[4-(phenylmethoxy)phenoxy]-(67856-23-9)

Safety Data

• Hazardous Substances Data: 67856-23-9(Hazardous Substances Data)

Upstream product

• 103-16-2 4-Benzyloxyphenol 
• 107-07-3 2-chloro-ethanol 
• 205381-75-5 4-benzyloxyphenoxyethyl tetrahydro-2H-pyran-2-yl ether 
• 38559-92-1 2-(4-Benzyloxyphenoxy)ethanoic acid 

Downstream Products

• 3351-59-5 2-(4-benzyloxyphenoxy)ethyl bromide 
• 179019-78-4 2-(4-(benzyloxy)phenoxy)ethyl 4-methylbenzenesulfonate 
• 220698-59-9 p-(2-chloroethoxy)benzyloxybenzene 
• 1333170-24-3 (6S)-6-{2-[4-benzyloxyphenoxy]ethoxy}-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine 
• 1333171-25-7 1-(benzyloxy)-4-(2-iodoethoxy)benzene 
• 13427-53-7 4-(2-hydroxyethoxy)-phenol 
• 90414-53-2 5'-O-<2-<4-(benzyloxy)phenoxy>ethyl>thymidine 
• 220698-60-2 methyl 3,5-bis<2-(p-benzyloxyphenoxy)ethoxy>benzoate 

Relevant articles and documents

PHENYL BENZYL ETHER DERIVATIVE AND PREPARATION METHOD AND APPLICATION THEREOF

Parts of compounds, after being labeled by radionuclide, of the phenyl benzyl ether derivative, are used as Aβ plaque imaging agent. The structural formula of the phenyl benzyl ether derivative is shown by formula (I). The present invention develops a kin

Synthesis of N,N'-Bis(thioacetoxyalkoxy)piperazine and its self-assembled monolayer (SAM) formation on gold electrode

A novel terminal thioacetate-substitued alkoxy piperazine was successfully synthesized from 4-(benzyloxy)phenol after six-step reaction and employed as the surface-active material in fabrication of self-assembled monolayers (SAMs). Cyclic voltammetric (CV) results showed that the SAM-modified gold electrode had special capacity in recognition for Fe3+.

Synthesis of a new class of difunctional tetraphenylene crown ethers

Three new substituted tetraphenylene crown ethers have been made. Bis(5- carbomethoxy-1,3-phenylene)-bis(p-phenylene)-(3x + 6)-crown-x, where x = 12, 16, and 20 (11b-11d) were synthesized via [1 + 1] cyclization of methyl 3,5- bis[ω-chloro(oligoethyleneoxy)]benzoates (13b-3d) with methyl 3,5-bis[ω- (p-hydroxyphenoxy)(oligoethyleneoxy)]benzoates (16b-6d) using K2CO3 as base and tetrabutylammonium iodide as a phase transfer agent in dimethylformamide (DMF). The corresponding 30-membered (x = 8) macrocycle 11a could not be made by this approach; only the elimination product, 3,5-bis(vinyloxy)benzoic acid (19), was isolated. 16a-16d were made via alkylation of p-benzyloxyphenol (14) with 13a-13d, respectively, followed by hydrogenolysis with Pd/C as catalyst. No complexation of these macrocycles with dibenzylammonium ions was detected by NMR spectroscopy, but weak complexation of 11d with a paraquat derivative was observed.