CAS 1668-01-5

1,2-Benzenediamine, 3,4-dichloro-

Description:

1,2-Benzenediamine, 3,4-dichloro- 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 4 positions of the aromatic ring. This compound is typically a solid at room temperature and may exhibit a range of physical properties such as solubility in organic solvents and moderate melting and boiling points. It is known for its applications in the synthesis of dyes, pigments, and other organic compounds due to its reactivity and functional groups. Additionally, 1,2-benzenediamine derivatives can be involved in various chemical reactions, including nucleophilic substitutions and coupling reactions. However, it is important to handle this compound with care, as it may pose health risks, including potential toxicity and environmental hazards. Proper safety measures should be observed when working with this substance in a laboratory setting.

Formula: C₆H₆Cl₂N₂

1,2-Benzenediamine, 3,4-dichloro-

CAS: 1668-01-5

Formula: C₆H₆Cl₂N₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 177.0312

Ref: IN-DA001WYT

3,4-Dichloro-1,2-benzenediamine

CAS: 1668-01-5

3,4-Dichloro-1,2-benzenediamine

Purity: 95%

Molecular weight: 177.03g/mol

Ref: 54-OR55268

3,4-Dichlorobenzene-1,2-diamine

CAS: 1668-01-5

Purity: 97%

Molecular weight: 177.0299988

Ref: 10-F621686

3,4-dichlorobenzene-1,2-diamine

CAS: 1668-01-5

3,4-dichlorobenzene-1,2-diamine is a high salt compound that binds to sulfatide and has a molecular weight of 3.2 kilodaltons. It is an agonist for the galactose receptor in muscle cells, which causes stimulation of biochemical properties in the cell. The compound has been shown to be synthetic and expressed in E. coli. 3,4-Dichlorobenzene-1,2-diamine is also used as an immunofluorescent probe for studying the function of galactose receptors in muscle cells. This compound can also be immobilized on polyacrylamide gels to study its interactions with sulfatide.

Formula: C₆H₆Cl₂N₂

Purity: Min. 95%

Molecular weight: 177.03 g/mol

Ref: 3D-BAA66801