CAS 39224-65-2
:4,5-dichloro-2-nitrophenol
Description:
4,5-Dichloro-2-nitrophenol is an organic compound characterized by the presence of two chlorine atoms and one nitro group attached to a phenolic ring. Its molecular structure features a phenol group where the chlorine substituents are located at the 4 and 5 positions, while the nitro group is positioned at the 2 position. This compound typically appears as a yellow to brown solid and is known for its moderate solubility in organic solvents and limited solubility in water. It exhibits properties such as being a weak acid due to the hydroxyl group, and it can participate in various chemical reactions, including electrophilic substitution and nucleophilic attack. 4,5-Dichloro-2-nitrophenol is often used in research and industrial applications, particularly in the synthesis of dyes and other chemical intermediates. However, it is important to handle this compound with care, as it may pose environmental and health risks, including potential toxicity to aquatic organisms. Proper safety measures should be observed when working with this substance.
Formula:C6H3Cl2NO3
InChI:InChI=1/C6H3Cl2NO3/c7-3-1-5(9(11)12)6(10)2-4(3)8/h1-2,10H
SMILES:c1c(c(cc(c1N(=O)=O)O)Cl)Cl
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
4,5-Dichloro-2-nitrophenol
CAS:Formula:C6H3Cl2NO3Purity:97%Color and Shape:SolidMolecular weight:207.99894,5-Dichloro-2-nitrophenol
CAS:4,5-Dichloro-2-nitrophenolFormula:C6H3Cl2NO3Purity:≥95%Color and Shape: dark orange solidMolecular weight:208.00g/mol4,5-Dichloro-2-nitrophenol
CAS:Formula:C6H3Cl2NO3Purity:97%Color and Shape:CrystallineMolecular weight:207.994,5-Dichloro-2-nitrophenol
CAS:Controlled ProductFormula:C6H3Cl2NO3Color and Shape:NeatMolecular weight:207.9995-Dichloro-2-nitrophenol
CAS:<p>5-Dichloro-2-nitrophenol is a chemical that is used as an immunomodulator, pesticide, or herbicide. It is activated by the body to form a reactive intermediate that can bind to DNA and create mutations. 5-Dichloro-2-nitrophenol has been shown to cause oxidative damage in cell cultures and other tissues, such as proximal tubules of the kidney. It also produces malondialdehyde oxidation products which are known to be cytotoxic. In addition, preincubation with 5-Dichloro-2-nitrophenol increases the sensitivity of cells to other oxidative stressors such as peroxides and hydrogen peroxide.</p>Formula:C6H3Cl2NO3Purity:Min. 95%Molecular weight:208 g/mol




