(E)-Bis(2,3,5,6-tetrachlorophenyl)diazene

Base Information

Chemical Name:(E)-Bis(2,3,5,6-tetrachlorophenyl)diazene
CAS No.:77131-62-5
Molecular Formula:C₁₂H₂Cl₈N₂
Molecular Weight:457.785
Hs Code.:
DSSTox Substance ID:DTXSID20506236

Synonyms:77131-62-5;(E)-Bis(2,3,5,6-tetrachlorophenyl)diazene;DTXSID20506236

Suppliers and Price of (E)-Bis(2,3,5,6-tetrachlorophenyl)diazene

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
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Total 0 raw suppliers

Chemical Property of (E)-Bis(2,3,5,6-tetrachlorophenyl)diazene

Chemical Property:

XLogP3:8.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:457.766719
Heavy Atom Count:22
Complexity:347

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(C(=C(C(=C1Cl)Cl)N=NC2=C(C(=CC(=C2Cl)Cl)Cl)Cl)Cl)Cl

Technology Process of (E)-Bis(2,3,5,6-tetrachlorophenyl)diazene

There total 5 articles about (E)-Bis(2,3,5,6-tetrachlorophenyl)diazene 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: 96.0%

: 64186-88-5
4,4'-diaminooctachloroazobenzene

: 77131-62-5
4H,4'H-octachloroazobenzene

Guidance literature:: With methanol;
DOI:10.1016/0040-4039(80)88083-X

Reference yield:

: 50919-43-2
2,3,5,6-tetrachloro-p-quinondiimine

: 77131-62-5
4H,4'H-octachloroazobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / 170 °C / Heating

2: 96 percent / methanol

With methanol;
DOI:10.1016/0040-4039(80)88083-X

Reference yield:

: 5924-75-4
2,3,5,6-tetrachloro-p-phenylenediamine

: 77131-62-5
4H,4'H-octachloroazobenzene

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / K₃Fe(CN)6, NaOH / benzene; H₂O

2: 90 percent / 170 °C / Heating

3: 96 percent / methanol

With methanol; sodium hydroxide; potassium hexacyanoferrate(III); In water; benzene;
DOI:10.1016/0040-4039(80)88083-X