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Naphthalene, 1-[(ethenyloxy)methyl]-

Base Information
  • Chemical Name:Naphthalene, 1-[(ethenyloxy)methyl]-
  • CAS No.:48140-70-1
  • Molecular Formula:C13H12O
  • Molecular Weight:
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80451233
  • Nikkaji Number:J801.442F
  • Wikidata:Q82271154
Naphthalene, 1-[(ethenyloxy)methyl]-

Synonyms:48140-70-1;Naphthalene, 1-[(ethenyloxy)methyl]-;(1-Naphthylmethyl)vinyl ether;SCHEMBL14803712;DTXSID80451233

Suppliers and Price of Naphthalene, 1-[(ethenyloxy)methyl]-
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Chemical Property of Naphthalene, 1-[(ethenyloxy)methyl]-
Chemical Property:
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:184.088815002
  • Heavy Atom Count:14
  • Complexity:188
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C=COCC1=CC=CC2=CC=CC=C21
Technology Process of Naphthalene, 1-[(ethenyloxy)methyl]-

There total 1 articles about Naphthalene, 1-[(ethenyloxy)methyl]- 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:
Guidance literature:
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; phosphorous acid trimethyl ester; In benzene; Heating;
DOI:10.1021/ja020761x
Guidance literature:
Multi-step reaction with 2 steps
1: 1.) (R)-(+)-1,1'-bi-2-naphthol-TiCl2(OPr-i)2 / 1) toluene, 50 deg C, 4 h; 2) toluene, -30 deg C, 12 h
2: 1.) lithium allyloxide, 2.) formic acid, Et3N, palladium(II) acetate, triphenylphosphine, 3.) DBU
With formic acid; (R)-(+)-1,1'-bi-2-naphthol titanium dichloride diisopropoxide; lithium allyl oxide; palladium diacetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; triphenylphosphine;
DOI:10.1021/jo9515900
Guidance literature:
Multi-step reaction with 2 steps
1: 86 percent / (R)-(+)-1,1'-bi-2-naphthol titanium dichloride diisopropoxide complex / toluene / 12 h / -30 °C
2: 98 percent
With (R)-(+)-1,1'-bi-2-naphthol titanium dichloride diisopropoxide; In toluene;
DOI:10.1016/S0040-4039(00)78338-9
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