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8-Oxononanoic acid

Base Information
  • Chemical Name:8-Oxononanoic acid
  • CAS No.:25542-64-7
  • Molecular Formula:C9H16O3
  • Molecular Weight:172.224
  • Hs Code.:2918300090
  • DSSTox Substance ID:DTXSID00948438
  • Nikkaji Number:J206.110D
  • Wikidata:Q82926269
  • Metabolomics Workbench ID:1644
  • Mol file:25542-64-7.mol
8-Oxononanoic acid

Synonyms:8-Oxononanoic acid;25542-64-7;8-oxo-nonanoic acid;8-Ketopelargonic acid;8-Oxononanoicacid;8-ketononanoic acid;LMFA01060159;SCHEMBL2342846;DTXSID00948438;CHEBI:179517;KNPGTJGXMGNBAY-UHFFFAOYSA-N;AKOS033384856;CS-0223931;EN300-117102;F87880;Z1262510893

Suppliers and Price of 8-Oxononanoic acid
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
  • TRC
  • 8-oxononanoicacid
  • 100mg
  • $ 330.00
  • AK Scientific
  • 8-Oxononanoicacid
  • 5g
  • $ 2613.00
Total 5 raw suppliers
Chemical Property of 8-Oxononanoic acid
Chemical Property:
  • PSA:54.37000 
  • LogP:2.00060 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:7
  • Exact Mass:172.109944368
  • Heavy Atom Count:12
  • Complexity:152
Purity/Quality:

99% *data from raw suppliers

8-oxononanoicacid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC(=O)CCCCCCC(=O)O
  • Uses 8-Oxononanoic Acid (CAS# 25542-64-7) is used in the preparation of a cancer vaccine comprising a synergistic combination of TLR-?9 agonist and a glycolipid-?peptide conjugate. It can also be used to synthesize 10-hydroxycamptothecine derivative useful in treatment of cancer as well as to synthesize glycolipid peptide conjugates for use as antimalarial vaccines.
Technology Process of 8-Oxononanoic acid

There total 19 articles about 8-Oxononanoic acid 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:
non-8-ynoic acid; With methanol; In 1,2-dichloro-ethane; at 20 ℃; for 3.5h; Inert atmosphere;
With silica gel; Inert atmosphere;
DOI:10.1246/cl.180610
Guidance literature:
With hydrogenchloride; sodium nitrite; In tetrahydrofuran; water; at -5 - 20 ℃; for 10h;
DOI:10.1021/acs.orglett.1c02327
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