1,4-Dichloro-2-nitrobenzene, 98%
1,4-Dichloro-2-nitrobenzene, 98%
1,4-Dichloro-2-nitrobenzene, 98%
Thermo Scientific Chemicals

1,4-Dichloro-2-nitrobenzene, 98%

CAS: 89-61-2 | C6H3Cl2NO2 | 192.00 g/mol
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Catalog number A11896.0E
also known as A11896-0E
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2500 g
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Chemical Identifiers
CAS89-61-2
IUPAC Name1,4-dichloro-2-nitrobenzene
Molecular FormulaC6H3Cl2NO2
InChI KeyRZKKOBGFCAHLCZ-UHFFFAOYSA-N
SMILES[O-][N+](=O)C1=CC(Cl)=CC=C1Cl
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder or lumps
Melting Point (clear melt)52.0-58.0?C
Appearance (Color)Pale yellow to yellow
Assay (GC)≥97.5%
1,4-Dichloro-2-nitrobenzene is a reagent used in the synthesis of antitrypanosomal, antileishmanial and antimalarial agents. It is also used in the synthesis of lysophosphatidic acid acyltransferase-β in hibitors.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1,4-Dichloro-2-nitrobenzene is a reagent used in the synthesis of antitrypanosomal, antileishmanial and antimalarial agents. It is also used in the synthesis of lysophosphatidic acid acyltransferase-β in hibitors.

Solubility
Soluble in water, ethanol, ether, benzene, carbon disulfide. Slightly soluble in carbon tetrachloride.

Notes
Incompatible with strong oxidizing agents, strong bases.
RUO – Research Use Only

General References:

  1. Makoto Ohnishi; Kazunori Yamazaki; Seigo Yamamoto; Taijiro Matsushima. Characterization of N-Acetylcysteine Conjugate in Yellow Urine by Oral Administration of 1,4-Dichloro-2-Nitrobenzene in Rats.Journal of Health Science. 2004, 50 319-322.
  2. Kumar; J Senthil; Arivazhagan M. DFT and ab-initio study of structure of 1,4-dichloro-2-nitrobenzene.Indian Journal of Pure & Applied Physics. 2011, 49 673-678.