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1-Hexacosene

Base Information
  • Chemical Name:1-Hexacosene
  • CAS No.:18835-33-1
  • Molecular Formula:C26H52
  • Molecular Weight:364.699
  • Hs Code.:2901299090
  • European Community (EC) Number:242-615-9,300-203-7
  • UNII:MSG4U9AQ89
  • DSSTox Substance ID:DTXSID80873052
  • Nikkaji Number:J129.612D
  • Wikidata:Q27284213
  • Metabolomics Workbench ID:5018
  • Mol file:18835-33-1.mol
1-Hexacosene

Synonyms:1-Hexacosene;hexacos-1-ene;18835-33-1;HEXACOSENE;UNII-MSG4U9AQ89;MSG4U9AQ89;EINECS 242-615-9;AI3-10513;EC 242-615-9;93924-11-9;Alkenes, C24-28 .alpha.-;DTXSID80873052;CHEBI:184289;C26H52;LMFA11000320;C26-H52;F87219;Q27284213

Suppliers and Price of 1-Hexacosene
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
Total 22 raw suppliers
Chemical Property of 1-Hexacosene
Chemical Property:
  • Vapor Pressure:0.009Pa at 25℃ 
  • Melting Point:51.8°C 
  • Refractive Index:1.4657 (estimate) 
  • Boiling Point:405.6°Cat760mmHg 
  • Flash Point:237.2°C 
  • PSA:0.00000 
  • Density:0.805g/cm3 
  • LogP:10.16460 
  • XLogP3:14.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:23
  • Exact Mass:364.406901659
  • Heavy Atom Count:26
  • Complexity:242
Purity/Quality:

99.9% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Chemical Classes:UVCB
  • Canonical SMILES:CCCCCCCCCCCCCCCCCCCCCCCCC=C
  • Uses 1-?Hexacosene is a part of Carica papaya peel extracts and may contain antibacterial activity.
Technology Process of 1-Hexacosene

There total 1 articles about 1-Hexacosene 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:
Triallylborane; dimethylsulfoxonium methylide; In toluene; at 80 ℃; for 0.25h;
With propionic acid; for 72h; Further byproducts given. Title compound not separated from byproducts; Heating;
DOI:10.1021/ma050152k
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