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2-Naphthyl glycidyl ether

Base Information Edit
  • Chemical Name:2-Naphthyl glycidyl ether
  • CAS No.:5234-06-0
  • Molecular Formula:C13H12 O2
  • Molecular Weight:200.237
  • Hs Code.:2910900090
  • European Community (EC) Number:226-030-6
  • UNII:TA1R9121W4
  • DSSTox Substance ID:DTXSID10966724
  • Nikkaji Number:J297.947K
  • Wikidata:Q27289860
  • ChEMBL ID:CHEMBL1929348
  • Mol file:5234-06-0.mol
2-Naphthyl glycidyl ether

Synonyms:5234-06-0;2-Naphthyl glycidyl ether;2-[(2-naphthyloxy)methyl]oxirane;2-Glycidyloxynaphthalene;2-((naphthalen-2-yloxy)methyl)oxirane;2-[(naphthalen-2-yloxy)methyl]oxirane;2-(naphthalen-2-yloxymethyl)oxirane;beta-Naphthyl glycidyl ether;Glycidyl beta-naphthyl ether;CCRIS 2070;((2-Naphthyloxy)methyl)oxirane;2-((2-naphthyloxy)methyl)-oxiran;Ether, 2,3-epoxypropyl 2-naphthyl;EINECS 226-030-6;Oxirane, ((2-naphthalenyloxy)methyl)-;(2-naphthyloxymethyl)oxirane;UNII-TA1R9121W4;AI3-13143;TA1R9121W4;MFCD00450019;Oxirane, 2-((2-naphthyloxy)methyl)-;Propane, 1,2-epoxy-3-(2-naphthyloxy)-;Naphthalene, 2-(2,3-expoxypropoxy)- (7CI,8CI);[(2-naphthyloxy)methyl]oxirane;2-((2-naphthyloxy)methyl)oxirane;2-[(2-Naphthalenyloxy)methyl]oxirane;2-((2-NAPHTHALENYLOXY)METHYL)OXIRANE;1-(2-naphthyloxy)-2,3-epoxypropane;2-naphtyl glycidyl ether;SCHEMBL844653;2-(2-naphthyloxymethyl)oxirane;CHEMBL1929348;DTXSID10966724;[(2-naphthalenyloxy)methyl]oxirane;2-[(2-naphthyloxy)methyl] oxirane;BBL011772;STK802541;AKOS000117494;AKOS016039349;GLYCIDYL .BETA.-NAPHTHYL ETHER;Naphthalene, 2-(2,3-expoxypropoxy)-;VS-03027;2-{[(Naphthalen-2-yl)oxy]methyl}oxirane;LS-101089;CS-0307892;2-NAPHTHYL GLYCIDYL ETHER, (+/-)-;EN300-09937;OXIRANE, 2-((2-NAPHTHALENYLOXY)METHYL)-;Propane, 1,2-epoxy-3-(2-naphthyloxy)- (6CI);SR-01000013299;SR-01000013299-1;Q27289860;F1574-0049;Z104494470

Suppliers and Price of 2-Naphthyl glycidyl ether
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 2-[(naphthalen-2-yloxy)methyl]oxirane
  • 500mg
  • $ 695.00
  • American Custom Chemicals Corporation
  • 2-[(2-NAPHTHYLOXY)METHYL]OXIRANE 95.00%
  • 5G
  • $ 1082.56
  • American Custom Chemicals Corporation
  • 2-[(2-NAPHTHYLOXY)METHYL]OXIRANE 95.00%
  • 2.5G
  • $ 906.27
  • American Custom Chemicals Corporation
  • 2-[(2-NAPHTHYLOXY)METHYL]OXIRANE 95.00%
  • 1G
  • $ 677.91
  • AK Scientific
  • 2-Naphthylglycidylether
  • 500mg
  • $ 271.00
  • AK Scientific
  • 2-Naphthylglycidylether
  • 100mg
  • $ 166.00
Total 8 raw suppliers
Chemical Property of 2-Naphthyl glycidyl ether Edit
Chemical Property:
  • Vapor Pressure:9.96E-05mmHg at 25°C 
  • Melting Point:60-64 °C 
  • Boiling Point:348.7°Cat760mmHg 
  • Flash Point:152°C 
  • PSA:21.76000 
  • Density:1.192g/cm3 
  • LogP:2.61740 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:200.083729621
  • Heavy Atom Count:15
  • Complexity:217
Purity/Quality:

99% *data from raw suppliers

2-[(naphthalen-2-yloxy)methyl]oxirane *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(O1)COC2=CC3=CC=CC=C3C=C2
  • Uses 2-[(naphthalen-2-yloxy)methyl]oxirane is a monoesters of ibuprofen where are used as prodrugs with analgesic activity
Technology Process of 2-Naphthyl glycidyl ether

There total 20 articles about 2-Naphthyl glycidyl ether 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 caesium carbonate; In acetonitrile; at 82 ℃; for 3h;
Guidance literature:
With tetraethylammonium perchlorate; triethylamine; In acetonitrile; electrolysis;
DOI:10.1016/S0040-4039(00)91658-7
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