CAS 1930-72-9
:4-Chloro-3,5-dinitrobenzonitrile
Description:
4-Chloro-3,5-dinitrobenzonitrile is an organic compound characterized by its aromatic structure, which includes a benzene ring substituted with a chlorine atom, two nitro groups, and a cyano group. The presence of the nitro groups, which are strong electron-withdrawing groups, significantly influences the compound's reactivity and properties. This compound is typically a yellow crystalline solid, exhibiting low solubility in water but higher solubility in organic solvents. It is known for its use in various chemical syntheses and as an intermediate in the production of agrochemicals and pharmaceuticals. The chlorine and nitro substituents contribute to its potential as a reactive electrophile in nucleophilic substitution reactions. Additionally, due to the presence of nitro groups, it may exhibit explosive properties under certain conditions, necessitating careful handling and storage. As with many nitro-containing compounds, it may pose environmental and health risks, thus requiring appropriate safety measures during its use and disposal.
Formula:C7H2ClN3O4
InChI:InChI=1S/C7H2ClN3O4/c8-7-5(10(12)13)1-4(3-9)2-6(7)11(14)15/h1-2H
InChI key:InChIKey=SCGDEDHSPCXGEC-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(Cl)C(N(=O)=O)=CC(C#N)=C1
Synonyms:- 1-Chloro-4-cyano-2,6-dinitrobenzene
- 3,5-Dinitro-4-chlorobenzonitrile
- 4-Chloro-3,5-dinitrobenzenenitrile
- Ai3-28718
- Benzonitrile, 4-chloro-3,5-dinitro-
- Brn 1990451
- Nsc 74453
- 4-Chloro-3,5-dinitrobenzonitrile
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Found 6 products.
4-Chloro-3,5-dinitrobenzonitrile
CAS:Formula:C7H2ClN3O4Purity:98%Color and Shape:SolidMolecular weight:227.56154-Chloro-3,5-dinitrobenzonitrile
CAS:Formula:C7H2ClN3O4Purity:>98.0%(GC)(T)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:227.564-Chloro-3,5-dinitrobenzonitrile
CAS:<p>4-Chloro-3,5-dinitrobenzonitrile is a mesomeric compound that has four amines and one nitro group. It is a dipole with chloride as the negative end and amine as the positive end. The reaction mechanism of this chemical is nucleophilic substitution. 4-Chloro-3,5-dinitrobenzonitrile reacts with an organic solvent to form a buffer. A buffer is an ionized solution that resists changes in pH when acid or base are added to it. This chemical also reacts with thionyl chloride to form hydrochloric acid, which can be used to leishmania parasites. 4-Chloro-3,5-dinitrobenzonitrile also reacts with an anion such as ClO4− or NO2− to form a salt such as chlorate or nitrate respectively.</p>Formula:C7H2ClN3O4Purity:Min. 95%Color and Shape:PowderMolecular weight:227.56 g/mol4-Chloro-3,5-dinitrobenzonitrile
CAS:Controlled Product<p>Stability Unstable in Solution<br>Applications 4-Chloro-3,5-dinitrobenzonitrile is a reagent used in the synthesis of lodoxamide (L469365). Lodoxamide is an antiallergic drug that acts as a mast cell stabilizer. It is effective in the treatment of allergic conjunctivitis and in decreasing vascular permeability.<br>References Ciprandi, G., et al.: Allergy, 51(12), 946-951 (1996); Bayer, Atilla., et al.: Ophthalmologica, 217(2), 119-123 (2003)<br></p>Formula:C7H2ClN3O4Color and Shape:NeatMolecular weight:227.56






