[2-(Methoxymethoxy)pent-4-en-2-yl]benzene

Base Information

Chemical Name:[2-(Methoxymethoxy)pent-4-en-2-yl]benzene
CAS No.:89726-95-4
Molecular Formula:C13H18O2
Molecular Weight:206.285
Hs Code.:
DSSTox Substance ID:DTXSID10533238
Nikkaji Number:J1.485.691I

Synonyms:89726-95-4;[2-(Methoxymethoxy)pent-4-en-2-yl]benzene;DTXSID10533238

Suppliers and Price of [2-(Methoxymethoxy)pent-4-en-2-yl]benzene

Supply Marketing:

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

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Chemical Property of [2-(Methoxymethoxy)pent-4-en-2-yl]benzene

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:206.130679813
Heavy Atom Count:15
Complexity:185

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC=C)(C1=CC=CC=C1)OCOC

Technology Process of [2-(Methoxymethoxy)pent-4-en-2-yl]benzene

There total 3 articles about [2-(Methoxymethoxy)pent-4-en-2-yl]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: 88.0%

: 556-56-9
allyl iodid

: 98877-58-8
1-(methoxymethoxy)-1-phenyl-1-(trimethylstannyl)ethane

: 89726-95-4
O-(methoxymethyl)-4-phenyl-1-penten-4-ol

Guidance literature:: With n-butyllithium; In 1,2-dimethoxyethane; at -78 ℃;
DOI:10.1021/ja00211a024

Reference yield: 88.0%

: 109-72-8,29786-93-4
n-butyllithium

: 98877-58-8
1-(methoxymethoxy)-1-phenyl-1-(trimethylstannyl)ethane

: 89726-95-4
O-(methoxymethyl)-4-phenyl-1-penten-4-ol

Guidance literature:: With allyl iodid; In 1,2-dimethoxyethane; under argon; tin-compound in DME cooled to -78 °C; nBuLi was added; quenched with allylhalide;; poured into NH4Cl-soln. and petroleum ether, shaked 1 min, organic layer sepd., washed (brine), dried (Na2SO4), filtered, concd. (vacuo); chromd. (silica gel; petroleum ether); NMR; IR; MAS;;
DOI:10.1021/ja00211a024