CAS 20734-67-2
:3,5-Dihydroxyaniline
Description:
3,5-Dihydroxyaniline, also known as 3,5-dihydroxy-aminobenzene, is an organic compound characterized by the presence of two hydroxyl (-OH) groups attached to the benzene ring at the 3 and 5 positions, along with an amino (-NH2) group. This compound is a derivative of aniline and exhibits properties typical of phenolic compounds, including solubility in water due to the hydroxyl groups. It is often used in the synthesis of dyes, pigments, and pharmaceuticals due to its ability to participate in various chemical reactions, such as electrophilic substitution and coupling reactions. The presence of multiple functional groups also allows for potential applications in polymer chemistry and as an intermediate in organic synthesis. Additionally, 3,5-dihydroxyaniline may exhibit antioxidant properties, making it of interest in biochemical research. Safety data should be consulted, as compounds with amino and hydroxyl groups can have varying degrees of toxicity and environmental impact.
Formula:C6H7NO2
InChI:InChI=1S/C6H7NO2/c7-4-1-5(8)3-6(9)2-4/h1-3,8-9H,7H2
InChI key:InChIKey=PDCMTKJRBAZZHL-UHFFFAOYSA-N
SMILES:NC1=CC(O)=CC(O)=C1
Synonyms:- 1,3-Benzenediol, 5-amino-
- 3,5-Dihydroxyaniline
- 5-Aminoresorcinol
- 5-Amino-1,3-benzenediol
- Resorcinol, 5-amino-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
5-Aminobenzene-1,3-diol
CAS:Controlled ProductFormula:C6H7NO2Color and Shape:NeatMolecular weight:125.1255-aminoresorcinol
CAS:<p>5-aminoresorcinol is a nucleophilic compound that can be used in oriented photocatalysis. It has good operational stability and high photoreactivity, with a hydroxyl group and an aromatic benzyl group. The product has been shown to have neutral pH levels, which is suitable for the environment. 5-Aminoresorcinol can be reused for photoelectron mineralization and nitrate reduction.</p>Formula:C6H7NO2Purity:Min. 95%Molecular weight:125.13 g/mol
