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Terephthalic acid, di(2-chloroethyl) ester

Base Information Edit
  • Chemical Name:Terephthalic acid, di(2-chloroethyl) ester
  • CAS No.:1026-93-3
  • Molecular Formula:C12H12Cl2O4
  • Molecular Weight:291.131
  • Hs Code.:
  • DSSTox Substance ID:DTXSID401193363
  • Nikkaji Number:J1.865.736H
  • Mol file:1026-93-3.mol
Terephthalic acid, di(2-chloroethyl) ester

Synonyms:Terephthalic acid, di(2-chloroethyl) ester;1026-93-3;SCHEMBL11233009;DBNYVAWEUHWAAQ-UHFFFAOYSA-N;DTXSID401193363;bis(2-chloroethyl) benzene-1,4-dicarboxylate;1,4-Benzenedicarboxylic acid, 1,4-bis(2-chloroethyl) ester

Suppliers and Price of Terephthalic acid, di(2-chloroethyl) ester
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 0 raw suppliers
Chemical Property of Terephthalic acid, di(2-chloroethyl) ester Edit
Chemical Property:
  • XLogP3:4.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:8
  • Exact Mass:290.0112642
  • Heavy Atom Count:18
  • Complexity:247
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC(=CC=C1C(=O)OCCCl)C(=O)OCCCl
Technology Process of Terephthalic acid, di(2-chloroethyl) ester

There total 2 articles about Terephthalic acid, di(2-chloroethyl) 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:
Guidance literature:
With 2,2'-azobis(isobutyronitrile); chloroform; In benzene; for 5h; Heating;
DOI:10.1080/00397919708005032
Guidance literature:
/BRN= 205356/, Cl2, (CH3O)3PO;
DOI:10.1021/jo01331a027
Guidance literature:
In acetone; at 55 ℃; for 5h; Time;
upstream raw materials:

1,4-bis(1,3-dioxolan-2-yl)benzene

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