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1,3-Diethyl 2-(2-buten-1-yl)propanedioate

Base Information Edit
  • Chemical Name:1,3-Diethyl 2-(2-buten-1-yl)propanedioate
  • CAS No.:7565-66-4
  • Molecular Formula:C11H18O4
  • Molecular Weight:214.262
  • Hs Code.:
  • DSSTox Substance ID:DTXSID101271815
  • Mol file:7565-66-4.mol
1,3-Diethyl 2-(2-buten-1-yl)propanedioate

Synonyms:DTXSID101271815;AKOS017562063;7565-66-4;1,3-Diethyl 2-(2-buten-1-yl)propanedioate

Suppliers and Price of 1,3-Diethyl 2-(2-buten-1-yl)propanedioate
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 1,3-Diethyl 2-(2-buten-1-yl)propanedioate Edit
Chemical Property:
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:8
  • Exact Mass:214.12050905
  • Heavy Atom Count:15
  • Complexity:215
Purity/Quality:

95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCOC(=O)C(CC=CC)C(=O)OCC
Technology Process of 1,3-Diethyl 2-(2-buten-1-yl)propanedioate

There total 1 articles about 1,3-Diethyl 2-(2-buten-1-yl)propanedioate 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:
With hexacarbonyl molybdenum; In 1,4-dioxane; at 110 ℃; for 48h; Yield given. Yields of byproduct given;
DOI:10.1016/S0040-4039(00)95751-4
Guidance literature:
Multi-step reaction with 2 steps
1: urea
2: 1-bromo-but-2-ene
With (E/Z)-crotyl bromide; urea;
Guidance literature:
Multi-step reaction with 2 steps
1: (i) EtONO, (ii) NaOEt
2: (i) Al-Hg, (ii) aq. NaOH
DOI:10.1039/j39710001305
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