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4-(2,3,4,6-Tetraiodophenoxy)crotonic acid methyl ester

Base Information
  • Chemical Name:4-(2,3,4,6-Tetraiodophenoxy)crotonic acid methyl ester
  • CAS No.:91058-69-4
  • Molecular Formula:C11H8I4O3
  • Molecular Weight:695.801
  • Hs Code.:
  • Wikidata:Q76327070
  • Mol file:91058-69-4.mol
4-(2,3,4,6-Tetraiodophenoxy)crotonic acid methyl ester

Synonyms:BRN 3154925;4-(2,3,4,6-Tetraiodophenoxy)crotonic acid methyl ester;gamma-(2,3,4,6-Tetrajodphenoxy) crotonsaeuremethyl ester [German];CROTONIC ACID, 4-(2,3,4,6-TETRAIODOPHENOXY)-, METHYL ESTER;91058-69-4;gamma-(2,3,4,6-Tetrajodphenoxy) crotonsaeuremethyl ester

Suppliers and Price of 4-(2,3,4,6-Tetraiodophenoxy)crotonic acid methyl ester
Supply Marketing:
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 4-(2,3,4,6-Tetraiodophenoxy)crotonic acid methyl ester
Chemical Property:
  • Vapor Pressure:9.46E-13mmHg at 25°C 
  • Boiling Point:564.2°C at 760 mmHg 
  • Flash Point:295°C 
  • Density:2.627g/cm3 
  • XLogP3:4.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:695.6652
  • Heavy Atom Count:18
  • Complexity:311
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC(=O)C=CCOC1=C(C(=C(C=C1I)I)I)I
  • Isomeric SMILES:COC(=O)/C=C/COC1=C(C(=C(C=C1I)I)I)I
Technology Process of 4-(2,3,4,6-Tetraiodophenoxy)crotonic acid methyl ester

There total 3 articles about 4-(2,3,4,6-Tetraiodophenoxy)crotonic 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:
Guidance literature:
Multi-step reaction with 3 steps
1: aqueous hydrobromic acid; acetic acid
2: iodine; methanol; aqueous hydrogen peroxide
3: sodium ethylate; ethanol
With methanol; ethanol; hydrogen bromide; dihydrogen peroxide; iodine; sodium ethanolate; acetic acid;
DOI:10.1002/ardp.19592921102
Guidance literature:
Multi-step reaction with 2 steps
1: iodine; methanol; aqueous hydrogen peroxide
2: sodium ethylate; ethanol
With methanol; ethanol; dihydrogen peroxide; iodine; sodium ethanolate;
DOI:10.1002/ardp.19592921102
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