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2,5-Nonanedione

Base Information Edit
  • Chemical Name:2,5-Nonanedione
  • CAS No.:25234-82-6
  • Molecular Formula:C9H16O2
  • Molecular Weight:156.225
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40456082
  • Nikkaji Number:J328.973G
  • Wikidata:Q82278290
  • Metabolomics Workbench ID:5610
  • Mol file:25234-82-6.mol
2,5-Nonanedione

Synonyms:2,5-nonanedione;Nonane-2,5-dione;Nonan-2,5-dione;25234-82-6;SCHEMBL8620315;DTXSID40456082;LWOMTZPPFKJNPA-UHFFFAOYSA-N;LMFA12000244

Suppliers and Price of 2,5-Nonanedione
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
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  • price
Total 0 raw suppliers
Chemical Property of 2,5-Nonanedione Edit
Chemical Property:
  • PSA:34.14000 
  • LogP:2.11490 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:6
  • Exact Mass:156.115029749
  • Heavy Atom Count:11
  • Complexity:139
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCC(=O)CCC(=O)C
Technology Process of 2,5-Nonanedione

There total 4 articles about 2,5-Nonanedione 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 triethylamine; 3-ethyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazolium bromide; In various solvent(s); at 80 ℃; for 10h;
DOI:10.1002/adsc.200404123
Guidance literature:
With di-tert-butyl diperoxyoxalate; oxygen; In benzene; at 45 ℃; for 4h; Product distribution; other hydroxyperoxides; also with subsequent LAH- or PPh3-reduction; also in the presence of alcohols; intra- and intermolecular hydrogen abstraction;
Guidance literature:
With platinum(IV) oxide; ethyl acetate; Hydrogenation;
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