Methyl 4-[(4-methoxyphenyl)methoxy]benzoate

Base Information

Chemical Name:Methyl 4-[(4-methoxyphenyl)methoxy]benzoate
CAS No.:62290-50-0
Molecular Formula:C16H16O4
Molecular Weight:272.301
Hs Code.:
DSSTox Substance ID:DTXSID70505633
Wikidata:Q82360874

Synonyms:Methyl 4-[(4-methoxyphenyl)methoxy]benzoate;62290-50-0;methyl-4-(4-methoxybenzyloxy)benzoate;SCHEMBL3729907;DTXSID70505633;HMDLADLMQPSLFT-UHFFFAOYSA-N;methyl 4(4-methoxybenzyloxy)benzoate;AKOS009100522;methyl 4-(4-methoxybenzyloxy)benzoate;4-(4-Methoxy-benzyloxy)-benzoic acid methyl ester

Suppliers and Price of Methyl 4-[(4-methoxyphenyl)methoxy]benzoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of Methyl 4-[(4-methoxyphenyl)methoxy]benzoate

Chemical Property:

PSA：44.76000
LogP:3.06080
XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:272.10485899
Heavy Atom Count:20
Complexity:289

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)COC2=CC=C(C=C2)C(=O)OC

Technology Process of Methyl 4-[(4-methoxyphenyl)methoxy]benzoate

There total 3 articles about Methyl 4-[(4-methoxyphenyl)methoxy]benzoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 86.0%

: 99-76-3,156291-94-0
methyl 4-hydroxylbenzoate

: 824-94-2
p-methoxybenzyl chloride

: 62290-50-0
methyl 4-(4-methoxybenzyloxy)benzoate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 17h; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.joc.0c02663