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5H-3,6-Methenofuro[3,2-G]oxireno[D]oxacycloundec

Base Information
  • Chemical Name:5H-3,6-Methenofuro[3,2-G]oxireno[D]oxacycloundec
  • CAS No.:10247-71-9
  • Molecular Formula:C15H16O6
  • Molecular Weight:292.288
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40874666
  • Mol file:10247-71-9.mol
5H-3,6-Methenofuro[3,2-G]oxireno[D]oxacycloundec

Synonyms:DTXSID40874666;5H-3,6-METHENOFURO[3,2-G]OXIRENO[D]OXACYCLOUNDEC

Suppliers and Price of 5H-3,6-Methenofuro[3,2-G]oxireno[D]oxacycloundec
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 5 raw suppliers
Chemical Property of 5H-3,6-Methenofuro[3,2-G]oxireno[D]oxacycloundec
Chemical Property:
  • PSA:85.36000 
  • LogP:0.24820 
  • XLogP3:0.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:292.09468823
  • Heavy Atom Count:21
  • Complexity:593
Purity/Quality:

98%,99%, *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC12CC3C=C(CC4C(C(C1O2)O)C(=C)C(=O)O4)C(=O)O3
Technology Process of 5H-3,6-Methenofuro[3,2-G]oxireno[D]oxacycloundec

There total 2 articles about 5H-3,6-Methenofuro[3,2-G]oxireno[D]oxacycloundec 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:

Reference yield:

Guidance literature:
Elephantopin (4), KOH, MeOH;
DOI:10.1021/jo01264a035

Reference yield:

Guidance literature:
Elephantopin 4, KOH/Methanol;
DOI:10.1021/jo01264a035
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