Benzenesulfonic acid, 5-chloro-2-(4-chloro-2-nitrophenoxy)-

Base Information

• Chemical Name: Benzenesulfonic acid, 5-chloro-2-(4-chloro-2-nitrophenoxy)-
• CAS No.: 68892-04-6
• Molecular Formula: C12H7 Cl2 N O6 S
• Molecular Weight: 364.163
• European Community (EC) Number: 272-592-0
• DSSTox Substance ID: DTXSID8071803
• Nikkaji Number: J332.666G
• Wikidata: Q81999598
• Mol file: 68892-04-6.mol

Synonyms:68892-04-6;5-Chloro-2-(4-chloro-2-nitrophenoxy)benzenesulfonic acid;Benzenesulfonic acid, 5-chloro-2-(4-chloro-2-nitrophenoxy)-;EINECS 272-592-0;5-Chloro-2-(4-chloro-2-nitrophenoxy)benzenesulphonic acid;C12H7Cl2NO6S;DTXSID8071803;SCHEMBL11427879;C12-H7-Cl2-N-O6-S

Chemical Property of Benzenesulfonic acid, 5-chloro-2-(4-chloro-2-nitrophenoxy)-

Chemical Property:

• PSA: 117.80000
• Density: 1.666g/cm³
• LogP: 5.54460
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 362.9371135
• Heavy Atom Count: 22
• Complexity: 505

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1Cl)[N+](=O)[O-])OC2=C(C=C(C=C2)Cl)S(=O)(=O)O

Technology Process of Benzenesulfonic acid, 5-chloro-2-(4-chloro-2-nitrophenoxy)-

There total 4 articles about Benzenesulfonic acid, 5-chloro-2-(4-chloro-2-nitrophenoxy)- 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:

4-chloro-1-(4-chlorophenoxy)-2-nitrobenzene (135-12-6) → 5-chloro-2-(4-chloro-2-nitro-phenoxy)-benzenesulfonic acid (68892-04-6)

Guidance literature:

With sulfuric acid;

Reference yield:

potassium 4-chlorophenoxide (1121-74-0) → 5-chloro-2-(4-chloro-2-nitro-phenoxy)-benzenesulfonic acid (68892-04-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 170 °C

2: H₂SO₄

With sulfuric acid;

Reference yield:

2,5-dichloronitrobenzene (89-61-2) → 5-chloro-2-(4-chloro-2-nitro-phenoxy)-benzenesulfonic acid (68892-04-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 170 °C

2: H₂SO₄

With sulfuric acid;

upstream raw materials:

4-chloro-1-(4-chlorophenoxy)-2-nitrobenzene

potassium 4-chlorophenoxide

2,5-dichloronitrobenzene

Downstream raw materials:

2-(2-amino-4-chloro-phenoxy)-5-chloro-benzenesulfonic acid

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