205381-75-5

Basic information

• Product Name: 4-benzyloxyphenoxyethyl tetrahydro-2H-pyran-2-yl ether
• Synonyms: 4-benzyloxyphenoxyethyl tetrahydro-2H-pyran-2-yl ether
• CAS NO: 205381-75-5
• Molecular Weight: 328.408
• Mol File: 205381-75-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-benzyloxyphenoxyethyl tetrahydro-2H-pyran-2-yl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 4-benzyloxyphenoxyethyl tetrahydro-2H-pyran-2-yl ether(205381-75-5)
• EPA Substance Registry System: 4-benzyloxyphenoxyethyl tetrahydro-2H-pyran-2-yl ether(205381-75-5)

Safety Data

• Hazardous Substances Data: 205381-75-5(Hazardous Substances Data)

Upstream product

• 17739-45-6 2-(2-bromoethoxy)tetrahydropyran 
• 103-16-2 4-Benzyloxyphenol 
• 5631-96-9 2-(2-chloroethoxy)-tetrahydro-2H-pyrane 

Downstream Products

• 1487428-87-4 4-(3-nitrophenoxy)phenoxyethyl tetrahydro-2H-pyran-2-yl ether 
• 1430408-53-9 4-(3-nitrophenoxy)phenoxyethanol 
• 1487428-88-5 4-(3-nitrophenoxy)phenoxyethyl 4-toluenesulfonate 
• 1487428-89-6 4-(3-nitrophenoxy)phenoxyethyl thiocyanate 
• 270261-91-1 4-hydroxyphenoxyethyl tetrahydro-2H-pyran-2-yl ether 
• 85983-09-1 4-[(3-trifluoro)phenoxy]phenoxyethanol 
• 179019-78-4 2-(4-(benzyloxy)phenoxy)ethyl 4-methylbenzenesulfonate 
• 220698-60-2 methyl 3,5-bis<2-(p-benzyloxyphenoxy)ethoxy>benzoate 

Relevant articles and documents

Aryloxyethyl thiocyanates are potent growth inhibitors of Trypanosoma cruzi and Toxoplasma gondii

Abstract As a part of our project aimed at searching for new safe chemotherapeutic agents against parasitic diseases, several compounds structurally related to the antiparasitic agent WC-9 (4-phenoxyphenoxyethyl thiocyanate), which were modified at the te

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.