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Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester

Base Information Edit
  • Chemical Name:Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester
  • CAS No.:32251-45-9
  • Molecular Formula:C15H16O7
  • Molecular Weight:308.28
  • Hs Code.:
  • Mol file:32251-45-9.mol
Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester

Synonyms:Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester

Suppliers and Price of Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester Edit
Chemical Property:
  • Melting Point:179 - 180.5 °C 
  • PSA:95.97000 
  • LogP:0.06290 
Purity/Quality:
Safty Information:
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  • Hazard Codes: 
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Technology Process of Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester

There total 2 articles about Decahydro-1,5-dimethyl-3,6,8-trioxo-1,5-methanobenzo[1,2-c:3,4-c']difuran-4-carboxylic acid methyl ester 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:
Trisaeurelacton 5a, 1.) O2, 2.) Pb(OAc)4, 3.) verd. HNO3, 4.) CH2N2;
DOI:10.1021/jo00966a033

Reference yield:

Guidance literature:
Trisaeurelacton 5a, 1.) Ac2O, 2.) CH2N2, 3.) H2O, 4.) O2, 5.) Pb(OAc)4, 6.) verd. HNO3;
DOI:10.1021/jo00966a033
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