{[(4,4-Dimethoxybutan-2-yl)oxy]methyl}benzene

Base Information

Chemical Name:{[(4,4-Dimethoxybutan-2-yl)oxy]methyl}benzene
CAS No.:95603-58-0
Molecular Formula:C₁₃H₂₀O₃
Molecular Weight:224.3
Hs Code.:
DSSTox Substance ID:DTXSID60537044

Synonyms:95603-58-0;{[(4,4-Dimethoxybutan-2-yl)oxy]methyl}benzene;DTXSID60537044

Suppliers and Price of {[(4,4-Dimethoxybutan-2-yl)oxy]methyl}benzene

Supply Marketing:

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

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Chemical Property of {[(4,4-Dimethoxybutan-2-yl)oxy]methyl}benzene

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:224.14124450
Heavy Atom Count:16
Complexity:163

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC(OC)OC)OCC1=CC=CC=C1

Technology Process of {[(4,4-Dimethoxybutan-2-yl)oxy]methyl}benzene

There total 1 articles about {[(4,4-Dimethoxybutan-2-yl)oxy]methyl}benzene 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:

: 39562-58-8
1,1-dimethoxybutan-3-ol

: 100-44-7
benzyl chloride

: 95603-58-0
3-(Phenylmethoxy)-butanal dimethyl acetal

Guidance literature:: With sodium hydride; Yield given. Multistep reaction; 1) dry DMSO, 30 min 2) 12h, room temperature;
DOI:10.1021/jo00196a022

Reference yield:

: 95603-58-0
3-(Phenylmethoxy)-butanal dimethyl acetal

: 762-72-1
allyl-trimethyl-silane

: ((1R,3R)-3-Methoxy-1-methyl-hex-5-enyloxymethyl)-benzene

: ((1R,3S)-3-Methoxy-1-methyl-hex-5-enyloxymethyl)-benzene

Guidance literature:: With titanium tetrachloride; isopropyl titanoate(IV); In dichloromethane; at -78 ℃; for 2h; Product distribution; Further Lewis acids; variation of temperatures, reaction times, and molar equvivalents of Lewis acid;
DOI:10.1016/S0040-4039(01)81596-3