CAS 42389-30-0
:5-Chloro-3-nitro-1,2-benzenediamine
Description:
5-Chloro-3-nitro-1,2-benzenediamine, with the CAS number 42389-30-0, is an organic compound that belongs to the class of aromatic amines. It features a benzene ring substituted with both a chlorine atom and a nitro group, along with two amino groups positioned at the 1 and 2 positions of the ring. This compound is typically characterized by its solid state at room temperature and may exhibit a yellow to brown coloration. It is known for its potential applications in dye manufacturing, as well as in the synthesis of various chemical intermediates. The presence of both amino and nitro groups contributes to its reactivity, making it a useful building block in organic synthesis. However, like many aromatic amines, it may pose health risks, including potential carcinogenicity, necessitating careful handling and appropriate safety measures during use. Its solubility in organic solvents and limited solubility in water are also notable characteristics, influencing its behavior in chemical reactions and applications.
Formula:C6H6ClN3O2
InChI:InChI=1S/C6H6ClN3O2/c7-3-1-4(8)6(9)5(2-3)10(11)12/h1-2H,8-9H2
InChI key:InChIKey=PIPKLZRJGNJMBY-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(N)C(N)=CC(Cl)=C1
Synonyms:- 5-Chloro-3-nitro-o-phenylenediamine
- 1,2-Benzenediamine, 5-chloro-3-nitro-
- 5-Chloro-3-nitro-1,2-phenylenediamine
- 5-Chloro-3-nitro-1,2-benzenediamine
- 3-Nitro-5-chloro-o-phenylenediamine
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100
Found 2 products.
5-Chloro-3-nitrobenzene-1,2-diamine
CAS:<p>5-Chloro-3-nitrobenzene-1,2-diamine is a cytotoxic compound that inhibits the activity of amino groups. It binds to an amino group on the target protein and prevents the formation of a hydrogen bond with an adjacent molecule, which leads to inhibition of protein synthesis. 5-Chloro-3-nitrobenzene-1,2-diamine has been shown to have inhibitory effects against quinoxalines and benzotriazoles.</p>Formula:C6H6ClN3O2Purity:Min. 95%Molecular weight:187.58 g/mol
