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(-)-1,2-Epoxydecane

Base Information Edit
  • Chemical Name:(-)-1,2-Epoxydecane
  • CAS No.:81623-66-7
  • Molecular Formula:C10H20O
  • Molecular Weight:
  • Hs Code.:
  • UNII:72X24OXG6J
  • Nikkaji Number:J941.218B
  • Wikidata:Q27266104
  • Mol file:81623-66-7.mol
(-)-1,2-Epoxydecane

Synonyms:(-)-1,2-Epoxydecane;Oxirane, 2-octyl-, (2S)-;(S)-2-Octyloxirane;81623-66-7;(S)-1,2-Epoxydecane;Oxirane, octyl-, (S)-;Oxirane, octyl-, (2S)-;1,2-Epoxydecane, (-)-;UNII-72X24OXG6J;72X24OXG6J;2beta-Octyloxirane;1,2(S)-epoxydecane;SCHEMBL3019229;AT36206;Q27266104

Suppliers and Price of (-)-1,2-Epoxydecane
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
Total 1 raw suppliers
Chemical Property of (-)-1,2-Epoxydecane Edit
Chemical Property:
  • XLogP3:4.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:7
  • Exact Mass:156.151415257
  • Heavy Atom Count:11
  • Complexity:90.9
Purity/Quality:

95% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCC1CO1
  • Isomeric SMILES:CCCCCCCC[C@H]1CO1
Technology Process of (-)-1,2-Epoxydecane

There total 6 articles about (-)-1,2-Epoxydecane 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 sodium methylate; In methanol; Yields of byproduct given. Title compound not separated from byproducts; Ambient temperature; e.e. 96percent;
Guidance literature:
With water; In neat (no solvent); at 0 - 20 ℃; for 8h; enantioselective reaction; Resolution of racemate;
DOI:10.1039/c4cy00594e
Guidance literature:
With Oxone; C6H10O6(C3H4)2; tetra(n-butyl)ammonium hydrogensulfate; edetate disodium; sodium hydrogencarbonate; In water; acetonitrile; at -10 ℃; for 1.5h; Product distribution; other reaction time, solvent, reagent;
DOI:10.1021/ja972272g
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