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Ethyl methyl cyclopropane-1,2-dicarboxylate

Base Information Edit
  • Chemical Name:Ethyl methyl cyclopropane-1,2-dicarboxylate
  • CAS No.:878-14-8
  • Molecular Formula:C8H12O4
  • Molecular Weight:
  • Hs Code.:
  • NSC Number:245494
  • DSSTox Substance ID:DTXSID10955355
  • Nikkaji Number:J478.690D
  • Mol file:878-14-8.mol
Ethyl methyl cyclopropane-1,2-dicarboxylate

Synonyms:33769-98-1;NSC245494;SCHEMBL24318092;DTXSID10955355;AKOS006282030;NSC-245494;Ethyl methyl cyclopropane-1,2-dicarboxylate;1-ETHYL 2-METHYL CYCLOPROPANE-1,2-DICARBOXYLATE

Suppliers and Price of Ethyl methyl cyclopropane-1,2-dicarboxylate
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
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of Ethyl methyl cyclopropane-1,2-dicarboxylate Edit
Chemical Property:
  • XLogP3:0.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:172.07355886
  • Heavy Atom Count:12
  • Complexity:199
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC(=O)C1CC1C(=O)OC
Technology Process of Ethyl methyl cyclopropane-1,2-dicarboxylate

There total 1 articles about Ethyl methyl cyclopropane-1,2-dicarboxylate 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:
Halbestersaeurechlorid /BRN= 947314/, Methanol;
DOI:10.1246/bcsj.50.1784
Guidance literature:
With sodium hydroxide; acetic anhydride; Multistep reaction; 1.) 15 h, reflux, 2.) 0.5 h, reflux;
DOI:10.1055/s-1983-30385
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