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Bis(2-ethoxyethyl) benzene-1,4-dicarboxylate

Base Information
  • Chemical Name:Bis(2-ethoxyethyl) benzene-1,4-dicarboxylate
  • CAS No.:32651-36-8
  • Molecular Formula:C16H22O6
  • Molecular Weight:310.347
  • Hs Code.:
  • DSSTox Substance ID:DTXSID30536463
  • Wikidata:Q82411122
Bis(2-ethoxyethyl) benzene-1,4-dicarboxylate

Synonyms:Bis-ethoxyethylterephthalat;Bis(2-ethoxyethyl) benzene-1,4-dicarboxylate;32651-36-8;SCHEMBL17797870;DTXSID30536463;PTINJMSTTLBEHT-UHFFFAOYSA-N;Terephthalic acid, di(2-ethoxyethyl) ester

Suppliers and Price of Bis(2-ethoxyethyl) benzene-1,4-dicarboxylate
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Bis(2-ethoxyethyl) benzene-1,4-dicarboxylate
Chemical Property:
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:12
  • Exact Mass:310.14163842
  • Heavy Atom Count:22
  • Complexity:291
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOCCOC(=O)C1=CC=C(C=C1)C(=O)OCCOCC
Technology Process of Bis(2-ethoxyethyl) benzene-1,4-dicarboxylate

There total 2 articles about Bis(2-ethoxyethyl) benzene-1,4-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:
With pyridine; In toluene; at 60 ℃; for 5.25h;
DOI:10.1016/j.chemosphere.2021.130005
Guidance literature:
Terephthaloyldichlorid, 2-Ethoxyethanol;
DOI:10.1002/apmc.1977.050650110
Guidance literature:
lead(II) stearate; at 160 ℃; Product distribution; Kinetics; rate of reaction;
DOI:10.1007/BF00809350
upstream raw materials:

2-ethoxy-ethanol

terephthaloyl chloride

Downstream raw materials:

bis(octadecyl) terephthalate

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