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1-(2,4-Dinitrophenyl)pyridinium chloride

Base Information
  • Chemical Name:1-(2,4-Dinitrophenyl)pyridinium chloride
  • CAS No.:4185-69-7
  • Deprecated CAS:40808-00-2,1228504-28-6
  • Molecular Formula:C11H8ClN3O4
  • Molecular Weight:281.655
  • Hs Code.:2933399090
  • European Community (EC) Number:224-059-9
  • NSC Number:16029
  • DSSTox Substance ID:DTXSID60884040
  • Mol file:4185-69-7.mol
1-(2,4-Dinitrophenyl)pyridinium chloride

Synonyms:4185-69-7;1-(2,4-Dinitrophenyl)pyridinium chloride;(2,4-Dinitrophenyl)pyridinium chloride;Zincke Salt;N-(2,4-Dinitrophenyl)pyridinium chloride;NSC 16029;Pyridinium, 1-(2,4-dinitrophenyl)-, chloride;1-(2,4-dinitrophenyl)pyridin-1-ium;chloride;EINECS 224-059-9;Pyridinium, 1-(2,4-dinitrophenyl)-, chloride (1:1);1-(2,4-dinitrophenyl)pyridin-1-ium chloride;1-(2,4-dinitrophenyl)pyridin-1-ium,chloride;1-(2,4-dinitrophenyl)pyridiniumchloride;C11H8N3O4.Cl;1-(2,4-dinitrophenyl)-1??-pyridin-1-ylium chloride;LCZC1703;SCHEMBL6131224;C11-H8-N3-O4.Cl;DTXSID60884040;NSC16029;MFCD00184241;MFCD00680506;NSC-16029;AKOS001013510;Pyridinium,4-dinitrophenyl)-, chloride;1-(2,4-Dinitrophenyl)pyridinium (Cl-);AS-63660;1-(2,4-dinitrophenyl)-pyridinium chloride;1-(2',4'-Dinitrophenyl)pyridinium chloride;CS-0179394;D4143;EN300-45333;D90256;Z56788801;1-(2,4-dinitrophenyl)-1lambda5-pyridin-1-ylium chloride

Suppliers and Price of 1-(2,4-Dinitrophenyl)pyridinium chloride
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
  • 1-(2,4-Dinitrophenyl)pyridin-1-iumChloride
  • 100mg
  • $ 75.00
  • TCI Chemical
  • 1-(2,4-Dinitrophenyl)pyridinium Chloride >98.0%(HPLC)(T)
  • 1g
  • $ 218.00
  • Biosynth Carbosynth
  • 1-(2,4-Dinitrophenyl)pyridinium Chloride
  • 2 g
  • $ 504.00
  • Biosynth Carbosynth
  • 1-(2,4-Dinitrophenyl)pyridinium Chloride
  • 1 g
  • $ 315.00
  • Biosynth Carbosynth
  • 1-(2,4-Dinitrophenyl)pyridinium Chloride
  • 500 mg
  • $ 200.00
  • Biosynth Carbosynth
  • 1-(2,4-Dinitrophenyl)pyridinium Chloride
  • 250 mg
  • $ 125.00
  • Biosynth Carbosynth
  • 1-(2,4-Dinitrophenyl)pyridinium Chloride
  • 100 mg
  • $ 65.00
  • American Custom Chemicals Corporation
  • 1-(2,4-DINITROPHENYL)PYRIDINIUM CHLORIDE 95.00%
  • 5G
  • $ 1168.42
  • American Custom Chemicals Corporation
  • 1-(2,4-DINITROPHENYL)PYRIDINIUM CHLORIDE 95.00%
  • 2.5G
  • $ 983.88
  • American Custom Chemicals Corporation
  • 1-(2,4-DINITROPHENYL)PYRIDINIUM CHLORIDE 95.00%
  • 1G
  • $ 721.57
Total 15 raw suppliers
Chemical Property of 1-(2,4-Dinitrophenyl)pyridinium chloride
Chemical Property:
  • Melting Point:191°C(dec.)(lit.) 
  • PSA:95.52000 
  • LogP:-0.16990 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:1
  • Exact Mass:281.0203334
  • Heavy Atom Count:19
  • Complexity:319
Purity/Quality:

98%,99%, *data from raw suppliers

1-(2,4-Dinitrophenyl)pyridin-1-iumChloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=[N+](C=C1)C2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-].[Cl-]
  • General Description 1-(2,4-Dinitrophenyl)pyridinium chloride, also known as Zincke salt, is a stable pyridinium derivative that reacts with nucleophiles such as sodium sulfite and nitromethanide ion. With sulfite, it forms a mixture of products via attack on either the dinitrophenyl ring or the pyridinium ring, with the ratio influenced by solvent polarity. Additionally, it reacts with nitromethanide to yield a dihydropyridine derivative, which can be further oxidized to a nitromethylpyridinium ion. These reactions highlight its utility in nucleophilic substitution and functionalization chemistry.
Technology Process of 1-(2,4-Dinitrophenyl)pyridinium chloride

There total 6 articles about 1-(2,4-Dinitrophenyl)pyridinium chloride 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 pyridine; In ethanol;
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