1,3-Dichlorodibenzofuran

Base Information

• Chemical Name: 1,3-Dichlorodibenzofuran
• CAS No.: 94538-00-8
• Molecular Formula: C12H6 Cl2 O
• Molecular Weight: 237.085
• Hs Code.: 2932999099
• UNII: G534MIG3FU
• DSSTox Substance ID: DTXSID70915455
• Nikkaji Number: J460.780E
• Wikidata: Q27278758
• Mol file: 94538-00-8.mol

Synonyms:1,3-dichlorodibenzofuran

Chemical Property of 1,3-Dichlorodibenzofuran

Chemical Property:

• Vapor Pressure: 6.5E-05mmHg at 25°C
• Boiling Point: 355.2°Cat760mmHg
• Flash Point: 168.6°C
• PSA: 13.14000
• Density: 1.442g/cm³
• LogP: 4.89280
• XLogP3: 4.9
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 235.9795702
• Heavy Atom Count: 15
• Complexity: 246

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C3=C(O2)C=C(C=C3Cl)Cl

Technology Process of 1,3-Dichlorodibenzofuran

There total 4 articles about 1,3-Dichlorodibenzofuran 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: 65.0%

2-(3,5-Dichlorophenoxy)benzene-1-diazonium tetrafluoroborate → 1,3-Dichlorodibenzofuran (94538-00-8)

Guidance literature:

With iron(II) sulfate; Heating;

DOI:10.1135/cccc20000862

Reference yield:

municipal waste → 2-chlorodibenzofuran (51230-49-0) + 4-chlorodibenzo[b,d]furan (74992-96-4) + 1,3-Dichlorodibenzofuran (94538-00-8) + 1,7-dichlorodibenzofuran (94538-02-0)

Guidance literature:

With oxygen; at 350 ℃; Further byproducts given. Title compound not separated from byproducts; Formation of xenobiotics;

DOI:10.1016/S0045-6535(00)00223-X

Reference yield:

Pentachlorophenol (87-86-5,67471-28-7) + 3-monochlorophenol (108-43-0) + 2,3,6-trichlorophenol (933-75-5) + 3,5-dichlorophenol (591-35-5) + 2,3,5,6-tetrachlorophenol (935-95-5) + phenol (108-95-2,27073-41-2) → 1,3-Dichlorodibenzofuran (94538-00-8)

Guidance literature:

With benzene; at 600 ℃; for 0.00111111h; Formation of xenobiotics;

DOI:10.1016/j.chemosphere.2004.01.002

upstream raw materials:

Pentachlorophenol

3-monochlorophenol

2,3,6-trichlorophenol

3,5-dichlorophenol

Downstream raw materials:

dibenzo[b,d]furan-3-carboxylic acid

Dibenzofuran-1-carboxylic acid

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