2,4,8-Trichlorodibenzofuran

Base Information

Chemical Name:2,4,8-Trichlorodibenzofuran
CAS No.:54589-71-8
Molecular Formula:C12H5 Cl3 O
Molecular Weight:271.53
Hs Code.:2932999099
European Community (EC) Number:259-248-5
UNII:ER7QB1460O
DSSTox Substance ID:DTXSID80203017
Nikkaji Number:J266.921H
Wikidata:Q27277314
Mol file:54589-71-8.mol

Synonyms:2,4,8-TCDF;2,4,8-trichlorodibenzofuran

Suppliers and Price of 2,4,8-Trichlorodibenzofuran

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

American Custom Chemicals Corporation
2,4,8-TRICHLORODIBENZOFURAN 95.00%
5MG
$ 504.75

Total 19 raw suppliers

Chemical Property of 2,4,8-Trichlorodibenzofuran

Chemical Property:

Vapor Pressure:7.52E-06mmHg at 25°C
Melting Point:154°C
Refractive Index:1.7120 (rough estimate)
Boiling Point:387.1°C at 760 mmHg
Flash Point:187.9°C
PSA：13.14000
Density:1.54g/cm³
LogP:5.54620
XLogP3:6.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:269.940598
Heavy Atom Count:16
Complexity:273

Purity/Quality:

99% ^*data from raw suppliers

2,4,8-TRICHLORODIBENZOFURAN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:C1=CC2=C(C=C1Cl)C3=C(O2)C(=CC(=C3)Cl)Cl
Uses 2,4,8-Trichlorodibenzofuran is a standard used in environmental testing and research such as in the study of the thermal decomposition of endosulfan and the resulting formation of PCDD/F environmental toxins.

Technology Process of 2,4,8-Trichlorodibenzofuran

There total 7 articles about 2,4,8-Trichlorodibenzofuran 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:

Reference yield: 100.0%

: 130480-85-2
Trifluoro-methanesulfonic acid 5-chloro-2-(2,4-dichloro-phenoxy)-phenyl ester

: 54589-71-8
2,4,8-trichlorodibenzofuran

Guidance literature:: In acetone; Irradiation;
DOI:10.1016/S0040-4020(01)86752-1

Reference yield: 0.6606%

: 106-48-9,82344-39-6
4-chloro-phenol

: 5409-83-6
2,8-dichlorodibenzofuran

: 54589-71-8
2,4,8-trichlorodibenzofuran

: 120-83-2,40477-79-0
2,4-dichlorophenol

: 88-06-2,67471-29-8
2,4,6-Trichlorophenol

Guidance literature:: With oxygen; silica gel; copper dichloride; at 425 ℃; Further byproducts.; Formation of xenobiotics;
DOI:10.1016/j.chemosphere.2007.10.036

Reference yield:

: 3380-34-5,88032-08-0
triclosan

: 54589-71-8
2,4,8-trichlorodibenzofuran

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / K₂CO₃ / acetone / Ambient temperature

2: 100 percent / acetone / Irradiation

With potassium carbonate; In acetone;
DOI:10.1016/S0040-4020(01)86752-1