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2-(1-Naphthyl)oxirane

Base Information
  • Chemical Name:2-(1-Naphthyl)oxirane
  • CAS No.:62222-40-6
  • Molecular Formula:C12H10O
  • Molecular Weight:170.211
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40977803
  • Nikkaji Number:J2.023.064I
2-(1-Naphthyl)oxirane

Synonyms:2-(naphthalen-1-yl)oxirane;2-(1-NAPHTHYL)OXIRANE;Oxirane, 1-naphthalenyl-;62222-40-6;2(1-naphthyl)oxirane;SCHEMBL2464189;DTXSID40977803;VEKOQDMCBFGHBI-UHFFFAOYSA-N;AKOS000141287;EN300-297404

Suppliers and Price of 2-(1-Naphthyl)oxirane
Supply Marketing:
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
  • American Custom Chemicals Corporation
  • 2-(NAPHTHALEN-1-YL)OXIRANE 95.00%
  • 5MG
  • $ 497.73
Total 5 raw suppliers
Chemical Property of 2-(1-Naphthyl)oxirane
Chemical Property:
  • Vapor Pressure:0.000721mmHg at 25°C 
  • Melting Point:54-55 °C 
  • Boiling Point:317.3°C at 760 mmHg 
  • Flash Point:140.9°C 
  • PSA:12.53000 
  • Density:1.193g/cm3 
  • LogP:2.91110 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:170.073164938
  • Heavy Atom Count:13
  • Complexity:190
Purity/Quality:

97% *data from raw suppliers

2-(NAPHTHALEN-1-YL)OXIRANE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(O1)C2=CC=CC3=CC=CC=C32
Technology Process of 2-(1-Naphthyl)oxirane

There total 12 articles about 2-(1-Naphthyl)oxirane 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:
1-vinylnaphthalene; With water; hydrogen bromide; In dimethyl sulfoxide; at 60 ℃; for 12h; Schlenk technique;
With sodium hydroxide; In tetrahydrofuran; water; dimethyl sulfoxide; for 0.5h; Cooling with ice;
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