3,5-Dichlorobenzene-1,2-diamine, with the CAS number 5233-04-5, is an organic compound characterized by the presence of two amino groups (-NH2) and two chlorine substituents on a benzene ring. Specifically, the amino groups are located at the 1 and 2 positions, while the chlorine atoms are positioned at the 3 and 5 positions relative to the amino groups. This compound is typically a solid at room temperature and may exhibit a crystalline structure. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic aromatic ring. 3,5-Dichlorobenzene-1,2-diamine is of interest in various chemical applications, including as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Its reactivity is influenced by the electron-donating nature of the amino groups and the electron-withdrawing effects of the chlorine atoms, which can affect its behavior in chemical reactions. Safety precautions should be taken when handling this compound, as it may pose health risks upon exposure.

3,5-dichlorobenzene-1,2-diamine

5233-04-5: 1,2-Benzenediamine, 3,5-Dichloro-

"3,5-Dichlorobenzene-1,2-Diamine"

(2-amino-3,5-dichlorophenyl)amine

3,5-Dichlorobenzene-1,2-diamine

3,5-Dichloro-1,2-diaminobenzene is a ligand that binds to transition metal ions such as nickel. It has been shown to be an effective inhibitor of the syncytial virus in cell culture. The synthesis of 3,5-dichloro-1,2-diaminobenzene from 3,5-dichloroaniline and hydrochloric acid can be achieved using the following reaction:

3,5-Dichloroaniline + HCl → 3,5-Dichloro-1,2-diaminobenzene + HNO3 

This compound is also a precursor for the synthesis of pyrazole derivatives.

CAS 5233-04-5: 3,5-dichlorobenzene-1,2-diamine

"3,5-Dichlorobenzene-1,2-Diamine"

Ref: 54-OR1010804

(2-amino-3,5-dichlorophenyl)amine

Ref: 10-F314103

3,5-Dichlorobenzene-1,2-diamine

Ref: IN-DA003ILB

3,5-Dichloro-1,2-diaminobenzene

Ref: 3D-FAA23304