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2,3-Dichloro-5-nitro-1,4-naphthoquinone

Base Information
  • Chemical Name:2,3-Dichloro-5-nitro-1,4-naphthoquinone
  • CAS No.:22360-86-7
  • Molecular Formula:C10H3Cl2NO4
  • Molecular Weight:272.044
  • Hs Code.:2914700090
  • European Community (EC) Number:634-516-8
  • DSSTox Substance ID:DTXSID10402657
  • Nikkaji Number:J510.016J
  • Wikidata:Q82206098
  • Mol file:22360-86-7.mol
2,3-Dichloro-5-nitro-1,4-naphthoquinone

Synonyms:2,3-Dichloro-5-nitro-1,4-naphthoquinone;22360-86-7;2,3-dichloro-5-nitronaphthalene-1,4-dione;2,3-dichloro-5-nitronaphthoquinone;2,3-dichloro-5-nitro-1,4-dihydronaphthalene-1,4-dione;1,4-Naphthalenedione,2,3-dichloro-5-nitro-;SCHEMBL1393393;DTXSID10402657;XAA36086;MFCD00192929;AKOS001593464;AS-64986;CS-0205298;D2428;1,4-Naphthalenedione, 2,3-dichloro-5-nitro-;T70590;EN300-7381690;2,3-dichloro-1,4-dihydro-1,4-dioxo-5-nitronaphthalene;Z2574926058

Suppliers and Price of 2,3-Dichloro-5-nitro-1,4-naphthoquinone
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
  • TRC
  • 2,3-Dichloro-5-nitro-1,4-naphthoquinone
  • 500mg
  • $ 110.00
  • TRC
  • 2,3-Dichloro-5-nitro-1,4-naphthoquinone
  • 100mg
  • $ 60.00
  • TCI Chemical
  • 2,3-Dichloro-5-nitro-1,4-naphthoquinone >97.0%(GC)
  • 5g
  • $ 209.00
  • Crysdot
  • 2,3-Dichloro-5-nitronaphthalene-1,4-dione 95+%
  • 25g
  • $ 450.00
  • American Custom Chemicals Corporation
  • 2,3-DICHLORO-5-NITRO-1,4-NAPHTHOQUINONE 95.00%
  • 5MG
  • $ 499.86
  • Alichem
  • 2,3-Dichloro-5-nitronaphthalene-1,4-dione
  • 25g
  • $ 444.92
  • AK Scientific
  • 2,3-Dichloro-5-nitro-1,4-naphthoquinone
  • 5g
  • $ 357.00
Total 13 raw suppliers
Chemical Property of 2,3-Dichloro-5-nitro-1,4-naphthoquinone
Chemical Property:
  • Melting Point:176 °C 
  • Boiling Point:400.2 °C at 760 mmHg 
  • Flash Point:195.9 °C 
  • PSA:79.96000 
  • Density:1.71 g/cm3 
  • LogP:3.18620 
  • Storage Temp.:Sealed in dry,Room Temperature 
  • XLogP3:3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:0
  • Exact Mass:270.9439130
  • Heavy Atom Count:17
  • Complexity:440
Purity/Quality:

97% *data from raw suppliers

2,3-Dichloro-5-nitro-1,4-naphthoquinone *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 20/21/22-36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC2=C(C(=C1)[N+](=O)[O-])C(=O)C(=C(C2=O)Cl)Cl
  • General Description 2,3-Dichloro-5-nitro-1,4-naphthoquinone (DClNNQ) forms electron donor-acceptor (CT) complexes with methyl-substituted anilines in chlorinated solvents, specifically exhibiting a 1:2 (acceptor:donor) stoichiometry rather than 1:1. The formation of these complexes is supported by spectrophotometric analysis, with consistent stoichiometry across different solvents (chloroform, dichloromethane, and 1,2-dichloroethane) and minor temperature variations. Thermodynamic and spectroscopic parameters confirm the stability and characteristics of these interactions, while the solvent environment influences the measured properties. The study highlights the compound's role as an electron acceptor in CT complexation with aniline derivatives.
Technology Process of 2,3-Dichloro-5-nitro-1,4-naphthoquinone

There total 11 articles about 2,3-Dichloro-5-nitro-1,4-naphthoquinone 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:
With sulfuric acid; nitric acid;
Guidance literature:
With iodine; chlorine; In acetic acid; Heating;
DOI:10.1021/jm00158a031
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